Canonical Allele Identifier: CA1129724965
Gene: ABO HGNC NCBI

Linked Data

gnomAD v3: 9-133274135-G-GAT
gnomAD v4: 9-133274135-G-GAT
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274136_133274137insTA , CM000671.2:g.133274136_133274137insTA GRCh38
NC_000009.11:g.136149552_136149553insTA , CM000671.1:g.136149552_136149553insTA GRCh37
NC_000009.10:g.135139373_135139374insTA NCBI36
NG_006669.1:g.3499_3500insAT
NG_006669.2:g.6079_6080insAT

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+1026_58+1027insAT
ENST00000647353.1:n.53+1026_53+1027insAT
ENST00000651471.1:n.63+1826_63+1827insAT
ENST00000679909.1:c.28+1026_28+1027insAT ENSP00000506089.1:n.28+1026_28+1027insAT
ENST00000453660.3:n.40+1026_40+1027insAT
ENST00000538324.2:c.28+1026_28+1027insAT ENSP00000483018.1:n.28+1026_28+1027insAT
ENST00000611156.4:c.28+1026_28+1027insAT ENSP00000483265.1:n.28+1026_28+1027insAT
NM_020469.2:c.28+1026_28+1027insAT NP_065202.2:n.28+1026_28+1027insAT
NM_020469.3:c.28+1026_28+1027insAT NP_065202.2:n.28+1026_28+1027insAT
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