Canonical Allele Identifier: CA1882582408
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257514_133257515delinsCA , CM000671.2:g.133257514_133257515delinsCA GRCh38
NC_000009.11:g.136132901_136132902delinsCA , CM000671.1:g.136132901_136132902delinsCA GRCh37
NC_000009.10:g.135122722_135122723delinsCA NCBI36
NG_006669.1:g.20153_20154delinsTG
NG_006669.2:g.22701_22702delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.297_298delinsTG
ENST00000647353.1:n.54-6363_54-6362delinsTG
ENST00000651471.1:n.329+527_329+528delinsTG
ENST00000679909.1:c.28+17647_28+17648delinsTG ENSP00000506089.1:n.28+17647_28+17648delinsTG
ENST00000453660.3:n.279_280delinsTG
ENST00000538324.2:c.265_266delinsTG ENSP00000483018.1:p.Trp89=
ENST00000611156.4:c.265_266delinsTG ENSP00000483265.1:p.Trp89=
NM_020469.2:c.268_269delinsTG NP_065202.2:p.Trp90=
NM_020469.3:c.268_269delinsTG NP_065202.2:p.Trp90=