Canonical Allele Identifier: CA136260413

Gene: H2BC4 H2BC3

Linked Data

• dbSNP Id: rs566687290
• gnomAD v2: 6-26107459-G-T
• gnomAD v3: 6-26107231-G-T
• gnomAD v4: 6-26107231-G-T
• MyVariant Identifiers: chr6:g.26107459G>T (hg19) ; chr6:g.26107231G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26107231G>T , CM000668.2:g.26107231G>T	GRCh38
NC_000006.11:g.26107459G>T , CM000668.1:g.26107459G>T	GRCh37
NC_000006.10:g.26215438G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707188.1:c.391-16197C>A (H2BC4)	ENSP00000516775.1:n.391-16197C>A
ENST00000629531.1:c.132+16542C>A (H2BC3)	ENSP00000486472.1:n.132+16542C>A