Canonical Allele Identifier: CA1882582298
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257440T= , CM000671.2:g.133257440T= GRCh38
NC_000009.11:g.136132827T= , CM000671.1:g.136132827T= GRCh37
NC_000009.10:g.135122648T= NCBI36
NG_006669.1:g.20228A=
NG_006669.2:g.22776A=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.372A=
ENST00000647353.1:n.54-6288A=
ENST00000651471.1:n.329+602A=
ENST00000679909.1:c.28+17722A= ENSP00000506089.1:n.28+17722A=
ENST00000453660.3:n.354A=
ENST00000538324.2:c.340A= ENSP00000483018.1:p.Thr114=
ENST00000611156.4:c.340A= ENSP00000483265.1:p.Thr114=
NM_020469.2:c.343A= NP_065202.2:p.Thr115=
NM_020469.3:c.343A= NP_065202.2:p.Thr115=