Canonical Allele Identifier: CA1129717532
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1834713045
gnomAD v3: 9-133261646-CG-C
gnomAD v4: 9-133261646-CG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133261647del , CM000671.2:g.133261647del GRCh38
NC_000009.11:g.136137050del , CM000671.1:g.136137050del GRCh37
NC_000009.10:g.135126871del NCBI36
NG_006669.1:g.16003del
NG_006669.2:g.18568del

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.129-273del
ENST00000647353.1:n.54-10495del
ENST00000651471.1:n.134-273del
ENST00000679909.1:c.28+13515del ENSP00000506089.1:n.28+13515del
ENST00000453660.3:n.111-273del
ENST00000538324.2:c.99-273del ENSP00000483018.1:n.99-273del
ENST00000611156.4:c.99-273del ENSP00000483265.1:n.99-273del
NM_020469.2:c.99-273del NP_065202.2:n.99-273del
NM_020469.3:c.99-273del NP_065202.2:n.99-273del
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