Canonical Allele Identifier: CA5306055
Gene: ABO HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1008708453

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133262144C>A , CM000671.2:g.133262144C>A GRCh38
NC_000009.10:g.135127368C>A NCBI36
NC_000009.11:g.136137547C>A , CM000671.1:g.136137547C>A GRCh37
NG_006669.1:g.15505G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.3:n.65G>T
ENST00000538324.2:c.53G>T ENSP00000483018.1:p.Arg18Leu
ENST00000611156.4:c.53G>T ENSP00000483265.1:p.Arg18Leu
NM_020469.2:c.53G>T NP_065202.2:p.Arg18Leu