Canonical Allele Identifier: CA1882580460
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256145_133256146delinsAG , CM000671.2:g.133256145_133256146delinsAG GRCh38
NC_000009.11:g.136131532_136131533delinsAG , CM000671.1:g.136131532_136131533delinsAG GRCh37
NC_000009.10:g.135121353_135121354delinsAG NCBI36
NG_006669.1:g.21522_21523delinsCT
NG_006669.2:g.24070_24071delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.614_615delinsCT
ENST00000647353.1:n.54-4994_54-4993delinsCT
ENST00000651471.1:n.540_541delinsCT
ENST00000679909.1:c.28+19016_28+19017delinsCT ENSP00000506089.1:n.28+19016_28+19017delinsCT
ENST00000453660.3:n.596_597delinsCT
ENST00000538324.2:c.582_583delinsCT ENSP00000483018.1:p.Phe194=
ENST00000611156.4:c.582_583delinsCT ENSP00000483265.1:p.Phe194=
NM_020469.2:c.585_586delinsCT NP_065202.2:p.Phe195=
NM_020469.3:c.585_586delinsCT NP_065202.2:p.Phe195=