Canonical Allele Identifier: CA1882580235

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256042C= , CM000671.2:g.133256042C=	GRCh38
NC_000009.11:g.136131429C= , CM000671.1:g.136131429C=	GRCh37
NC_000009.10:g.135121250C=	NCBI36
NG_006669.1:g.21626G=
NG_006669.2:g.24174G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.718G=
ENST00000647353.1:n.54-4890G=
ENST00000679909.1:c.28+19120G=	ENSP00000506089.1:n.28+19120G=
ENST00000453660.3:n.700G=
ENST00000538324.2:c.686G=	ENSP00000483018.1:p.Gly229=
ENST00000611156.4:c.686G=	ENSP00000483265.1:p.Gly229=
NM_020469.2:c.689G=	NP_065202.2:p.Gly230=
NM_020469.3:c.689G=	NP_065202.2:p.Gly230=