Canonical Allele Identifier: CA1882584418

Gene: ABO

Linked Data

• dbSNP Id: rs1834683876

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133260227T>C , CM000671.2:g.133260227T>C	GRCh38
NC_000009.11:g.136135631T>C , CM000671.1:g.136135631T>C	GRCh37
NC_000009.10:g.135125452T>C	NCBI36
NG_006669.1:g.17423A>G
NG_006669.2:g.19988A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.186-361A>G
ENST00000647353.1:n.54-9075A>G
ENST00000651471.1:n.191-361A>G
ENST00000679909.1:c.28+14935A>G	ENSP00000506089.1:n.28+14935A>G
ENST00000453660.3:n.168-361A>G
ENST00000538324.2:c.156-361A>G	ENSP00000483018.1:n.156-361A>G
ENST00000611156.4:c.156-361A>G	ENSP00000483265.1:n.156-361A>G
NM_020469.2:c.156-361A>G	NP_065202.2:n.156-361A>G
NM_020469.3:c.156-361A>G	NP_065202.2:n.156-361A>G