Canonical Allele Identifier: CA375685433

Gene: ABO

Linked Data

• dbSNP Id: rs1434969032
• gnomAD v2: 9-136131405-C-T
• gnomAD v4: 9-133256018-C-T
• MyVariant Identifiers: chr9:g.136131405C>T (hg19) ; chr9:g.133256018C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256018C>T , CM000671.2:g.133256018C>T	GRCh38
NC_000009.11:g.136131405C>T , CM000671.1:g.136131405C>T	GRCh37
NC_000009.10:g.135121226C>T	NCBI36
NG_006669.1:g.21650G>A
NG_006669.2:g.24198G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.742G>A
ENST00000647353.1:n.54-4866G>A
ENST00000679909.1:c.28+19144G>A	ENSP00000506089.1:n.28+19144G>A
ENST00000453660.3:n.724G>A
ENST00000538324.2:c.710G>A	ENSP00000483018.1:p.Gly237Glu
ENST00000611156.4:c.710G>A	ENSP00000483265.1:p.Gly237Glu
NM_020469.2:c.713G>A	NP_065202.2:p.Gly238Glu
NM_020469.3:c.713G>A	NP_065202.2:p.Gly238Glu