Canonical Allele Identifier: CA1129716258
Gene: ABO HGNC NCBI

Linked Data

gnomAD v3: 9-133257992-A-AAGG
gnomAD v4: 9-133257992-A-AAGG
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257992_133257993insAGG , CM000671.2:g.133257992_133257993insAGG GRCh38
NG_006669.2:g.22222_22223insCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.269+104_269+105insCCT
ENST00000647353.1:n.54-6841_54-6840insCCT
ENST00000651471.1:n.329+49_329+50insCCT
ENST00000679909.1:c.28+17169_28+17170insCCT ENSP00000506089.1:n.28+17169_28+17170insCCT
ENST00000453660.3:n.251+104_251+105insCCT
ENST00000538324.2:c.239+104_239+105insCCT ENSP00000483018.1:n.239+104_239+105insCCT
ENST00000611156.4:c.239+104_239+105insCCT ENSP00000483265.1:n.239+104_239+105insCCT
NM_020469.2:c.239+104_239+105insCCT NP_065202.2:n.239+104_239+105insCCT
NM_020469.3:c.239+104_239+105insCCT NP_065202.2:n.239+104_239+105insCCT
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