Canonical Allele Identifier: CA1882580682

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256223G= , CM000671.2:g.133256223G=	GRCh38
NC_000009.11:g.136131610G= , CM000671.1:g.136131610G=	GRCh37
NC_000009.10:g.135121431G=	NCBI36
NG_006669.1:g.21445C=
NG_006669.2:g.23993C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.537C=
ENST00000647353.1:n.54-5071C=
ENST00000651471.1:n.463C=
ENST00000679909.1:c.28+18939C=	ENSP00000506089.1:n.28+18939C=
ENST00000453660.3:n.519C=
ENST00000538324.2:c.505C=	ENSP00000483018.1:p.Leu169=
ENST00000611156.4:c.505C=	ENSP00000483265.1:p.Leu169=
NM_020469.2:c.508C=	NP_065202.2:p.Leu170=
NM_020469.3:c.508C=	NP_065202.2:p.Leu170=