Canonical Allele Identifier: CA136260357
Gene: H2BC4 HGNC NCBI
H2BC3 HGNC NCBI

Linked Data

dbSNP Id: rs761054903
gnomAD v2: 6-26107429-T-C
gnomAD v3: 6-26107201-T-C
gnomAD v4: 6-26107201-T-C
MyVariant Identifiers: chr6:g.26107429T>C (hg19) chr6:g.26107201T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107201T>C , CM000668.2:g.26107201T>C GRCh38
NC_000006.11:g.26107429T>C , CM000668.1:g.26107429T>C GRCh37
NC_000006.10:g.26215408T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000707188.1:c.391-16167A>G (H2BC4) ENSP00000516775.1:n.391-16167A>G
ENST00000629531.1:c.132+16572A>G (H2BC3) ENSP00000486472.1:n.132+16572A>G
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