H2BC1 H2B clustered histone 1
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 32 |
Ranking
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0 |
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32 |
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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
[No Data.]
Locus Zoom
Variants
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 |
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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 | H2BFU |
SYNONYM | HIST1H2BA |
SYNONYM | STBP |
SYNONYM | TH2B |
SYNONYM | TSH2B |
SYNONYM | TSH2B.1 |
SYNONYM | bA317E16.3 |
SYNONYM | hTSH2B |
MIM | 609904 OMIM |
HGNC | HGNC:18730 HGNC |
Ensembl | ENSG00000146047 Ensembl |
AllianceGenome | HGNC:18730 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000274764.5 | hg38 | chr6 | 25,726,777 | 25,727,345 | 569 |
ENST00000274764.5 | hg19 | chr6 | 25,727,005 | 25,727,573 | 569 |
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