Canonical Allele Identifier: CA1882582286
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257434C= , CM000671.2:g.133257434C= GRCh38
NC_000009.11:g.136132821C= , CM000671.1:g.136132821C= GRCh37
NC_000009.10:g.135122642C= NCBI36
NG_006669.1:g.20234G=
NG_006669.2:g.22782G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.378G=
ENST00000647353.1:n.54-6282G=
ENST00000651471.1:n.329+608G=
ENST00000679909.1:c.28+17728G= ENSP00000506089.1:n.28+17728G=
ENST00000453660.3:n.360G=
ENST00000538324.2:c.346G= ENSP00000483018.1:p.Gly116=
ENST00000611156.4:c.346G= ENSP00000483265.1:p.Gly116=
NM_020469.2:c.349G= NP_065202.2:p.Gly117=
NM_020469.3:c.349G= NP_065202.2:p.Gly117=