Canonical Allele Identifier: CA136260346

Gene: H2BC4 H2BC3

Linked Data

• dbSNP Id: rs564877257
• gnomAD v2: 6-26107408-G-A
• gnomAD v3: 6-26107180-G-A
• gnomAD v4: 6-26107180-G-A
• MyVariant Identifiers: chr6:g.26107408G>A (hg19) ; chr6:g.26107180G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26107180G>A , CM000668.2:g.26107180G>A	GRCh38
NC_000006.11:g.26107408G>A , CM000668.1:g.26107408G>A	GRCh37
NC_000006.10:g.26215387G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707188.1:c.391-16146C>T (H2BC4)	ENSP00000516775.1:n.391-16146C>T
ENST00000629531.1:c.132+16593C>T (H2BC3)	ENSP00000486472.1:n.132+16593C>T