Canonical Allele Identifier: CA1882580433

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256136G= , CM000671.2:g.133256136G=	GRCh38
NC_000009.11:g.136131523G= , CM000671.1:g.136131523G=	GRCh37
NC_000009.10:g.135121344G=	NCBI36
NG_006669.1:g.21532C=
NG_006669.2:g.24080C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.624C=
ENST00000647353.1:n.54-4984C=
ENST00000651471.1:n.550C=
ENST00000679909.1:c.28+19026C=	ENSP00000506089.1:n.28+19026C=
ENST00000453660.3:n.606C=
ENST00000538324.2:c.592C=	ENSP00000483018.1:p.Arg198=
ENST00000611156.4:c.592C=	ENSP00000483265.1:p.Arg198=
NM_020469.2:c.595C=	NP_065202.2:p.Arg199=
NM_020469.3:c.595C=	NP_065202.2:p.Arg199=