Canonical Allele Identifier: CA1882579953
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255942_133255943delinsGA , CM000671.2:g.133255942_133255943delinsGA GRCh38
NC_000009.11:g.136131329_136131330delinsGA , CM000671.1:g.136131329_136131330delinsGA GRCh37
NC_000009.10:g.135121150_135121151delinsGA NCBI36
NG_006669.1:g.21725_21726delinsTC
NG_006669.2:g.24273_24274delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.817_818delinsTC
ENST00000647353.1:n.54-4791_54-4790delinsTC
ENST00000679909.1:c.28+19219_28+19220delinsTC ENSP00000506089.1:n.28+19219_28+19220deli...
ENST00000453660.3:n.799_800delinsTC
ENST00000538324.2:c.785_786delinsTC ENSP00000483018.1:p.Phe262=
ENST00000611156.4:c.785_786delinsTC ENSP00000483265.1:p.Phe262=
NM_020469.2:c.788_789delinsTC NP_065202.2:p.Phe263=
NM_020469.3:c.788_789delinsTC NP_065202.2:p.Phe263=