Canonical Allele Identifier: CA1882582323
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257464_133257465delinsCG , CM000671.2:g.133257464_133257465delinsCG GRCh38
NC_000009.11:g.136132851_136132852delinsCG , CM000671.1:g.136132851_136132852delinsCG GRCh37
NC_000009.10:g.135122672_135122673delinsCG NCBI36
NG_006669.1:g.20203_20204delinsCG
NG_006669.2:g.22751_22752delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.347_348delinsCG
ENST00000647353.1:n.54-6313_54-6312delinsCG
ENST00000651471.1:n.329+577_329+578delinsCG
ENST00000679909.1:c.28+17697_28+17698delinsCG ENSP00000506089.1:n.28+17697_28+17698delinsCG
ENST00000453660.3:n.329_330delinsCG
ENST00000538324.2:c.315_316delinsCG ENSP00000483018.1:p.Asn105=
ENST00000611156.4:c.315_316delinsCG ENSP00000483265.1:p.Asn105=
NM_020469.2:c.318_319delinsCG NP_065202.2:p.Asn106=
NM_020469.3:c.318_319delinsCG NP_065202.2:p.Asn106=