H2BC26 H2B clustered histone 26
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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20 |
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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
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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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 | H2BU1 |
SYNONYM | H2Bb |
SYNONYM | HIST3H2BB |
MIM | 615046 OMIM |
HGNC | HGNC:20514 HGNC |
Ensembl | ENSG00000196890 Ensembl |
AllianceGenome | HGNC:20514 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000620438.2 | hg38 | chr1 | 228,458,103 | 228,463,104 | 5,002 |
ENST00000693095.1 | hg38 | chr1 | 228,458,103 | 228,458,558 | 456 |
ENST00000693095.1 | hg19 | chr1 | 228,645,804 | 228,646,259 | 456 |
ENST00000620438.2 | hg19 | chr1 | 228,645,804 | 228,650,805 | 5,002 |
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