H2BC15 H2B clustered histone 15
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 5 | 0 |
Uncertain significance | 0 | 6 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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6 |
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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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | H2B/d |
SYNONYM | H2BFD |
SYNONYM | HIST1H2BN |
MIM | 602801 OMIM |
HGNC | HGNC:4749 HGNC |
Ensembl | ENSG00000233822 Ensembl |
AllianceGenome | HGNC:4749 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000612898.2 | hg38 | chr6 | 27,838,569 | 27,839,110 | 542 |
ENST00000606613.1 | hg38 | chr6 | 27,838,601 | 27,855,709 | 17,109 |
ENST00000612898.2 | hg19 | chr6 | 27,806,347 | 27,806,888 | 542 |
ENST00000606613.1 | hg19 | chr6 | 27,806,379 | 27,823,487 | 17,109 |
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