Canonical Allele Identifier: CA2840263423
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258140_133258141insA , CM000671.2:g.133258140_133258141insA GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-9_234-8insT
ENST00000647353.1:n.54-6989_54-6988insT
ENST00000651471.1:n.239-9_239-8insT
ENST00000679909.1:c.28+17021_28+17022insT ENSP00000506089.1:n.28+17021_28+17022insT
ENST00000453660.3:n.216-9_216-8insT
ENST00000538324.2:c.204-9_204-8insT ENSP00000483018.1:n.204-9_204-8insT
ENST00000611156.4:c.204-9_204-8insT ENSP00000483265.1:n.204-9_204-8insT
NM_020469.2:c.204-9_204-8insT NP_065202.2:n.204-9_204-8insT
NM_020469.3:c.204-9_204-8insT NP_065202.2:n.204-9_204-8insT