Canonical Allele Identifier: CA1882580170

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256023G= , CM000671.2:g.133256023G=	GRCh38
NC_000009.11:g.136131410G= , CM000671.1:g.136131410G=	GRCh37
NC_000009.10:g.135121231G=	NCBI36
NG_006669.1:g.21645C=
NG_006669.2:g.24193C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.737C=
ENST00000647353.1:n.54-4871C=
ENST00000679909.1:c.28+19139C=	ENSP00000506089.1:n.28+19139C=
ENST00000453660.3:n.719C=
ENST00000538324.2:c.705C=	ENSP00000483018.1:p.Phe235=
ENST00000611156.4:c.705C=	ENSP00000483265.1:p.Phe235=
NM_020469.2:c.708C=	NP_065202.2:p.Phe236=
NM_020469.3:c.708C=	NP_065202.2:p.Phe236=