H2BC21 H2B clustered histone 21
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 14 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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14 |
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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
Search Word
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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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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 |
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | GL105 |
SYNONYM | H2B |
SYNONYM | H2B-GL105 |
SYNONYM | H2B.1 |
SYNONYM | H2BE |
SYNONYM | H2BFQ |
SYNONYM | H2BGL105 |
SYNONYM | H2BQ |
SYNONYM | HIST2H2BE |
MIM | 601831 OMIM |
HGNC | HGNC:4760 HGNC |
Ensembl | ENSG00000184678 Ensembl |
AllianceGenome | HGNC:4760 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000369155.4 | hg38 | chr1 | 149,884,459 | 149,886,682 | 2,224 |
ENST00000369155.4 | hg19 | chr1 | 149,856,009 | 149,858,232 | 2,224 |
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