Canonical Allele Identifier: CA2692330629
Gene: ABO HGNC NCBI

Linked Data

gnomAD v4: 9-133257633-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257635del , CM000671.2:g.133257635del GRCh38
NC_000009.11:g.136133022del , CM000671.1:g.136133022del GRCh37
NC_000009.10:g.135122843del NCBI36
NG_006669.1:g.20033del
NG_006669.2:g.22581del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-92del
ENST00000647353.1:n.54-6482del
ENST00000651471.1:n.329+408del
ENST00000679909.1:c.28+17528del ENSP00000506089.1:n.28+17528del
ENST00000453660.3:n.252-92del
ENST00000538324.2:c.240-92del ENSP00000483018.1:n.240-92del
ENST00000611156.4:c.240-92del ENSP00000483265.1:n.240-92del
NM_020469.2:c.240-92del NP_065202.2:n.240-92del
NM_020469.3:c.240-92del NP_065202.2:n.240-92del
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