Canonical Allele Identifier: CA1882580511

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256161C= , CM000671.2:g.133256161C=	GRCh38
NC_000009.11:g.136131548C= , CM000671.1:g.136131548C=	GRCh37
NC_000009.10:g.135121369C=	NCBI36
NG_006669.1:g.21507G=
NG_006669.2:g.24055G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.599G=
ENST00000647353.1:n.54-5009G=
ENST00000651471.1:n.525G=
ENST00000679909.1:c.28+19001G=	ENSP00000506089.1:n.28+19001G=
ENST00000453660.3:n.581G=
ENST00000538324.2:c.567G=	ENSP00000483018.1:p.Glu189=
ENST00000611156.4:c.567G=	ENSP00000483265.1:p.Glu189=
NM_020469.2:c.570G=	NP_065202.2:p.Glu190=
NM_020469.3:c.570G=	NP_065202.2:p.Glu190=