Canonical Allele Identifier: CA1882582094
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257148_133257149delinsAG , CM000671.2:g.133257148_133257149delinsAG GRCh38
NC_000009.11:g.136132535_136132536delinsAG , CM000671.1:g.136132535_136132536delinsAG GRCh37
NC_000009.10:g.135122356_135122357delinsAG NCBI36
NG_006669.1:g.20519_20520delinsCT
NG_006669.2:g.23067_23068delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+260_403+261delinsCT
ENST00000647353.1:n.54-5997_54-5996delinsCT
ENST00000651471.1:n.330-793_330-792delinsCT
ENST00000679909.1:c.28+18013_28+18014delinsCT ENSP00000506089.1:n.28+18013_28+18014deli...
ENST00000453660.3:n.385+260_385+261delinsCT
ENST00000538324.2:c.371+260_371+261delinsCT ENSP00000483018.1:n.371+260_371+261delins...
ENST00000611156.4:c.371+260_371+261delinsCT ENSP00000483265.1:n.371+260_371+261delins...
NM_020469.2:c.374+260_374+261delinsCT NP_065202.2:n.374+260_374+261delinsCT
NM_020469.3:c.374+260_374+261delinsCT NP_065202.2:n.374+260_374+261delinsCT