Canonical Allele Identifier: CA1882580989

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256341C= , CM000671.2:g.133256341C=	GRCh38
NC_000009.11:g.136131728C= , CM000671.1:g.136131728C=	GRCh37
NC_000009.10:g.135121549C=	NCBI36
NG_006669.1:g.21327G=
NG_006669.2:g.23875G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.419G=
ENST00000647353.1:n.54-5189G=
ENST00000651471.1:n.345G=
ENST00000679909.1:c.28+18821G=	ENSP00000506089.1:n.28+18821G=
ENST00000453660.3:n.401G=
ENST00000538324.2:c.387G=	ENSP00000483018.1:p.Leu129=
ENST00000611156.4:c.387G=	ENSP00000483265.1:p.Leu129=
NM_020469.2:c.390G=	NP_065202.2:p.Leu130=
NM_020469.3:c.390G=	NP_065202.2:p.Leu130=