Canonical Allele Identifier: CA1882582497
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257572_133257573delinsTG , CM000671.2:g.133257572_133257573delinsTG GRCh38
NC_000009.11:g.136132959_136132960delinsTG , CM000671.1:g.136132959_136132960delinsTG GRCh37
NC_000009.10:g.135122780_135122781delinsTG NCBI36
NG_006669.1:g.20094_20095delinsCA
NG_006669.2:g.22642_22643delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-31_270-30delinsCA
ENST00000647353.1:n.54-6421_54-6420delinsCA
ENST00000651471.1:n.329+469_329+470delinsCA
ENST00000679909.1:c.28+17589_28+17590delinsCA ENSP00000506089.1:n.28+17589_28+17590delinsCA
ENST00000453660.3:n.252-31_252-30delinsCA
ENST00000538324.2:c.240-31_240-30delinsCA ENSP00000483018.1:n.240-31_240-30delinsCA
ENST00000611156.4:c.240-31_240-30delinsCA ENSP00000483265.1:n.240-31_240-30delinsCA
NM_020469.2:c.240-31_240-30delinsCA NP_065202.2:n.240-31_240-30delinsCA
NM_020469.3:c.240-31_240-30delinsCA NP_065202.2:n.240-31_240-30delinsCA