Canonical Allele Identifier: CA1882579382

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255731C= , CM000671.2:g.133255731C=	GRCh38
NC_000009.11:g.136131118C= , CM000671.1:g.136131118C=	GRCh37
NC_000009.10:g.135120939C=	NCBI36
NG_006669.1:g.21937G=
NG_006669.2:g.24485G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1029G=
ENST00000647353.1:n.54-4579G=
ENST00000679909.1:c.28+19431G=	ENSP00000506089.1:n.28+19431G=
ENST00000453660.3:n.1011G=
ENST00000538324.2:c.997G=	ENSP00000483018.1:p.Ala333=
ENST00000611156.4:c.997G=	ENSP00000483265.1:p.Ala333=
NM_020469.2:c.1000G=	NP_065202.2:p.Ala334=
NM_020469.3:c.1000G=	NP_065202.2:p.Ala334=