Canonical Allele Identifier: CA1882582331

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257465G= , CM000671.2:g.133257465G=	GRCh38
NC_000009.11:g.136132852G= , CM000671.1:g.136132852G=	GRCh37
NC_000009.10:g.135122673G=	NCBI36
NG_006669.1:g.20203C=
NG_006669.2:g.22751C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.347C=
ENST00000647353.1:n.54-6313C=
ENST00000651471.1:n.329+577C=
ENST00000679909.1:c.28+17697C=	ENSP00000506089.1:n.28+17697C=
ENST00000453660.3:n.329C=
ENST00000538324.2:c.315C=	ENSP00000483018.1:p.Asn105=
ENST00000611156.4:c.315C=	ENSP00000483265.1:p.Asn105=
NM_020469.2:c.318C=	NP_065202.2:p.Asn106=
NM_020469.3:c.318C=	NP_065202.2:p.Asn106=