H2BC11 H2B clustered histone 11
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| not provided | 4 | 0 |
| Uncertain significance | 0 | 16 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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16 |
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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
Search Word
| 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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
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MGeND data only
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| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | H2B/r |
| SYNONYM | H2BFR |
| SYNONYM | H2BJ |
| SYNONYM | HIST1H2BJ |
| MIM | 615044 OMIM |
| HGNC | HGNC:4761 HGNC |
| Ensembl | ENSG00000124635 Ensembl |
| AllianceGenome | HGNC:4761 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000607124.1 | hg38 | chr6 | 27,125,897 | 27,132,750 | 6,854 |
| ENST00000339812.3 | hg38 | chr6 | 27,132,316 | 27,132,795 | 480 |
| ENST00000607124.1 | hg19 | chr6 | 27,093,676 | 27,100,529 | 6,854 |
| ENST00000339812.3 | hg19 | chr6 | 27,100,095 | 27,100,574 | 480 |
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