Canonical Allele Identifier: CA467852810

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131377C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255990C>T , CM000671.2:g.133255990C>T	GRCh38
NC_000009.11:g.136131377C>T , CM000671.1:g.136131377C>T	GRCh37
NC_000009.10:g.135121198C>T	NCBI36
NG_006669.1:g.21678G>A
NG_006669.2:g.24226G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.770G>A
ENST00000647353.1:n.54-4838G>A
ENST00000679909.1:c.28+19172G>A	ENSP00000506089.1:n.28+19172G>A
ENST00000453660.3:n.752G>A
ENST00000538324.2:c.738G>A	ENSP00000483018.1:p.Glu246=
ENST00000611156.4:c.738G>A	ENSP00000483265.1:p.Glu246=
NM_020469.2:c.741G>A	NP_065202.2:p.Glu247=
NM_020469.3:c.741G>A	NP_065202.2:p.Glu247=