Canonical Allele Identifier: CA1882582848
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257862_133257863delinsCA , CM000671.2:g.133257862_133257863delinsCA GRCh38
NC_000009.11:g.136133249_136133250delinsCA , CM000671.1:g.136133249_136133250delinsCA GRCh37
NC_000009.10:g.135123070_135123071delinsCA NCBI36
NG_006669.1:g.19804_19805delinsTG
NG_006669.2:g.22352_22353delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.269+234_269+235delinsTG
ENST00000647353.1:n.54-6711_54-6710delinsTG
ENST00000651471.1:n.329+179_329+180delinsTG
ENST00000679909.1:c.28+17299_28+17300delinsTG ENSP00000506089.1:n.28+17299_28+17300delinsTG
ENST00000453660.3:n.251+234_251+235delinsTG
ENST00000538324.2:c.239+234_239+235delinsTG ENSP00000483018.1:n.239+234_239+235delinsTG
ENST00000611156.4:c.239+234_239+235delinsTG ENSP00000483265.1:n.239+234_239+235delinsTG
NM_020469.2:c.239+234_239+235delinsTG NP_065202.2:n.239+234_239+235delinsTG
NM_020469.3:c.239+234_239+235delinsTG NP_065202.2:n.239+234_239+235delinsTG