Canonical Allele Identifier: CA1882579286

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255691T= , CM000671.2:g.133255691T=	GRCh38
NC_000009.11:g.136131078T= , CM000671.1:g.136131078T=	GRCh37
NC_000009.10:g.135120899T=	NCBI36
NG_006669.1:g.21977A=
NG_006669.2:g.24525A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1069A=
ENST00000647353.1:n.54-4539A=
ENST00000679909.1:c.28+19471A=	ENSP00000506089.1:n.28+19471A=
ENST00000453660.3:n.1051A=
ENST00000538324.2:c.1037A=	ENSP00000483018.1:p.Asn346=
ENST00000611156.4:c.1037A=	ENSP00000483265.1:p.Asn346=
NM_020469.2:c.1040A=	NP_065202.2:p.Asn347=
NM_020469.3:c.1040A=	NP_065202.2:p.Asn347=