Canonical Allele Identifier: CA1882582829

Gene: ABO

Linked Data

• dbSNP Id: rs1834631428

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257843C>G , CM000671.2:g.133257843C>G	GRCh38
NC_000009.11:g.136133230C>G , CM000671.1:g.136133230C>G	GRCh37
NC_000009.10:g.135123051C>G	NCBI36
NG_006669.1:g.19824G>C
NG_006669.2:g.22372G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.269+254G>C
ENST00000647353.1:n.54-6691G>C
ENST00000651471.1:n.329+199G>C
ENST00000679909.1:c.28+17319G>C	ENSP00000506089.1:n.28+17319G>C
ENST00000453660.3:n.251+254G>C
ENST00000538324.2:c.239+254G>C	ENSP00000483018.1:n.239+254G>C
ENST00000611156.4:c.239+254G>C	ENSP00000483265.1:n.239+254G>C
NM_020469.2:c.239+254G>C	NP_065202.2:n.239+254G>C
NM_020469.3:c.239+254G>C	NP_065202.2:n.239+254G>C