Canonical Allele Identifier: CA591377581
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs782363139

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256370G>T , CM000671.2:g.133256370G>T GRCh38
NC_000009.11:g.136131757G>T , CM000671.1:g.136131757G>T GRCh37
NC_000009.10:g.135121578G>T NCBI36
NG_006669.1:g.21298C>A
NG_006669.2:g.23846C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.404-14C>A
ENST00000647353.1:n.54-5218C>A
ENST00000651471.1:n.330-14C>A
ENST00000679909.1:c.28+18792C>A ENSP00000506089.1:n.28+18792C>A
ENST00000453660.3:n.386-14C>A
ENST00000538324.2:c.372-14C>A ENSP00000483018.1:n.372-14C>A
ENST00000611156.4:c.372-14C>A ENSP00000483265.1:n.372-14C>A
NM_020469.2:c.375-14C>A NP_065202.2:n.375-14C>A
NM_020469.3:c.375-14C>A NP_065202.2:n.375-14C>A