Canonical Allele Identifier: CA1882579762

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255889G= , CM000671.2:g.133255889G=	GRCh38
NC_000009.11:g.136131276G= , CM000671.1:g.136131276G=	GRCh37
NC_000009.10:g.135121097G=	NCBI36
NG_006669.1:g.21779C=
NG_006669.2:g.24327C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.871C=
ENST00000647353.1:n.54-4737C=
ENST00000679909.1:c.28+19273C=	ENSP00000506089.1:n.28+19273C=
ENST00000453660.3:n.853C=
ENST00000538324.2:c.839C=	ENSP00000483018.1:p.Thr280=
ENST00000611156.4:c.839C=	ENSP00000483265.1:p.Thr280=
NM_020469.2:c.842C=	NP_065202.2:p.Thr281=
NM_020469.3:c.842C=	NP_065202.2:p.Thr281=