Canonical Allele Identifier: CA2786163232

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257297A>G , CM000671.2:g.133257297A>G	GRCh38
NC_000009.11:g.136132684A>G , CM000671.1:g.136132684A>G	GRCh37
NC_000009.10:g.135122505A>G	NCBI36
NG_006669.1:g.20371T>C
NG_006669.2:g.22919T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.403+112T>C
ENST00000647353.1:n.54-6145T>C
ENST00000651471.1:n.329+745T>C
ENST00000679909.1:c.28+17865T>C	ENSP00000506089.1:n.28+17865T>C
ENST00000453660.3:n.385+112T>C
ENST00000538324.2:c.371+112T>C	ENSP00000483018.1:n.371+112T>C
ENST00000611156.4:c.371+112T>C	ENSP00000483265.1:n.371+112T>C
NM_020469.2:c.374+112T>C	NP_065202.2:n.374+112T>C
NM_020469.3:c.374+112T>C	NP_065202.2:n.374+112T>C