Canonical Allele Identifier: CA1882580658

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256209C= , CM000671.2:g.133256209C=	GRCh38
NC_000009.11:g.136131596C= , CM000671.1:g.136131596C=	GRCh37
NC_000009.10:g.135121417C=	NCBI36
NG_006669.1:g.21459G=
NG_006669.2:g.24007G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.551G=
ENST00000647353.1:n.54-5057G=
ENST00000651471.1:n.477G=
ENST00000679909.1:c.28+18953G=	ENSP00000506089.1:n.28+18953G=
ENST00000453660.3:n.533G=
ENST00000538324.2:c.519G=	ENSP00000483018.1:p.Glu173=
ENST00000611156.4:c.519G=	ENSP00000483265.1:p.Glu173=
NM_020469.2:c.522G=	NP_065202.2:p.Glu174=
NM_020469.3:c.522G=	NP_065202.2:p.Glu174=