chr7:87439765:G>A Detail (hg38) (ABCB4)

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Summary
Information
Links
Disease area statistics
MGeND
ClinVar
CIViC
DisGeNET
Annotation
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Information

Genome

Assembly	Position
hg19	chr7:87,069,081-87,069,081 View the variant detail on this assembly version.
hg38	chr7:87,439,765-87,439,765

HGVS

ABCB4

Type	Transcript	Protein
RefSeq	NM_018849.2:c.1633C>T	NP_061337.1:p.Arg545Cys
	NM_000443.3:c.1633C>T	NP_000434.1:p.Arg545Cys
Ensemble	ENST00000265723.8:c.1633C>T	ENST00000265723.8:p.Arg545Cys
	ENST00000359206.8:c.1633C>T	ENST00000359206.8:p.Arg545Cys
	ENST00000453593.5:c.1633C>T	ENST00000453593.5:p.Arg545Cys
	ENST00000649586.2:c.1633C>T	ENST00000649586.2:p.Arg545Cys

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star	[No Data.]
Show details

Links

ABCB4

Type	Database	ID	Link
Gene	MIM	171060	OMIM
	HGNC	45	HGNC
	Ensembl	ENSG00000005471	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

[No Data.]

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.120	cholecystitis	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NA	DisGeNET	Detail

Overlapped Transcript Coordinates

Gene	Transcript ID	Exon Number	Chromosome	Start	Stop	Type	Amino Mutation	Transcript Position	Links

Overlapped Transcript

Gene	Transcript ID	Chromosome	Start	Stop	Links

Gene: -
dbSNP: rs397514620 dbSNP
Genome: hg38
Position: chr7:87,439,765-87,439,765
Variant Type: snv
Reference Allele: G
Alternative Allele: A

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