HLA-B major histocompatibility complex, class I, B

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
Locus Zoom
Variants
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Information

Symbol: HLA-B
Type: protein-coding
Description: major histocompatibility complex, class I, B
Entrez Gene ID: 3106
Genome: hg19
Position: chr6:31,321,652-31,334,844
Genome: hg38
Position: chr6:31,353,875-31,367,067
MIM: 142830 OMIM
HGNC: HGNC:4932 HGNC
Ensembl: ENSG00000234745 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	20
Likely benign	0	34
not provided	118	0

Ranking

	ClinVar
	0
	0
	0
	54
	0

Frequency

EXAC_EAS

EXAC_EAS

HGVD

HGVD

TOMMO

TOMMO

Gene

Position

EXAC_EAS

EXAC_EAS

HGVD

HGVD

TOMMO

TOMMO

Gene

Position

Disease area statistics

Locus Zoom

Variants

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Target data	:	MGeND data only
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Variant name	Gene	AA change	CDS	Japanese frequency	TogoVar	MGeND				Genome	ClinVar			CIViC evidence	DisGeNET entry	COSMIC occurrence	Prediction
Variant name	Gene	AA change	CDS	Japanese frequency	TogoVar	Entry	Origin	Type	Annotation	Genome	Entry	Origin	Annotation	CIViC evidence	DisGeNET entry	COSMIC occurrence	Prediction

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Target data	:	MGeND data only
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Name	MGeND				Type	Genome	Size	Chromosome	Start	Stop	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry
Name	Entry	Origin	Type	Annotation	Type	Genome	Size	Chromosome	Start	Stop	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

Search Word

Target data	:	MGeND data only
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Name	MGeND				Type	Genome	Gene symbol	Chromosome	Genomic start	Genomic stop	Strand	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry
Name	Entry	Origin	Type	Annotation	Type	Genome	Gene symbol	Chromosome	Genomic start	Genomic stop	Strand	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

Type	ID
SYNONYM	AS
SYNONYM	B-4901
SYNONYM	HLAB
MIM	142830 OMIM
HGNC	HGNC:4932 HGNC
Ensembl	ENSG00000234745 Ensembl
AllianceGenome	HGNC:4932

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000640094.2	hg38	chr6	31,354,483	31,357,158	2,676
ENST00000696559.1	hg38	chr6	31,353,875	31,367,028	13,154
ENST00000696562.1	hg38	chr6	31,353,882	31,367,040	13,159
ENST00000696561.1	hg38	chr6	31,353,882	31,366,856	12,975
ENST00000696560.1	hg38	chr6	31,353,875	31,367,067	13,193
ENST00000412585.7	hg38	chr6	31,353,875	31,357,179	3,305
ENST00000412585.7	hg19	chr6	31,321,652	31,324,956	3,305
ENST00000696559.1	hg19	chr6	31,321,652	31,334,805	13,154
ENST00000696560.1	hg19	chr6	31,321,652	31,334,844	13,193
ENST00000696561.1	hg19	chr6	31,321,659	31,334,633	12,975
ENST00000696562.1	hg19	chr6	31,321,659	31,334,817	13,159
ENST00000640094.2	hg19	chr6	31,322,260	31,324,935	2,676

Key	Value
strand	-
start	31,321,642
Gene Symbol	HLA-B
Entrez GeneId	3,106
Chr Band	6p21.3
end	31,325,021
chr	chr6

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