Canonical Allele Identifier: CA136260403

Gene: H2BC4 H2BC3

Linked Data

• dbSNP Id: rs963740192
• gnomAD v2: 6-26107452-G-A
• gnomAD v3: 6-26107224-G-A
• gnomAD v4: 6-26107224-G-A
• MyVariant Identifiers: chr6:g.26107452G>A (hg19) ; chr6:g.26107224G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26107224G>A , CM000668.2:g.26107224G>A	GRCh38
NC_000006.11:g.26107452G>A , CM000668.1:g.26107452G>A	GRCh37
NC_000006.10:g.26215431G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707188.1:c.391-16190C>T (H2BC4)	ENSP00000516775.1:n.391-16190C>T
ENST00000629531.1:c.132+16549C>T (H2BC3)	ENSP00000486472.1:n.132+16549C>T