Canonical Allele Identifier: CA1882580533

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256169G= , CM000671.2:g.133256169G=	GRCh38
NC_000009.11:g.136131556G= , CM000671.1:g.136131556G=	GRCh37
NC_000009.10:g.135121377G=	NCBI36
NG_006669.1:g.21499C=
NG_006669.2:g.24047C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.591C=
ENST00000647353.1:n.54-5017C=
ENST00000651471.1:n.517C=
ENST00000679909.1:c.28+18993C=	ENSP00000506089.1:n.28+18993C=
ENST00000453660.3:n.573C=
ENST00000538324.2:c.559C=	ENSP00000483018.1:p.Arg187=
ENST00000611156.4:c.559C=	ENSP00000483265.1:p.Arg187=
NM_020469.2:c.562C=	NP_065202.2:p.Arg188=
NM_020469.3:c.562C=	NP_065202.2:p.Arg188=