Canonical Allele Identifier: CA2579497376
Gene: ABO HGNC NCBI

Linked Data

gnomAD v4: 9-133257617-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257622del , CM000671.2:g.133257622del GRCh38
NC_000009.11:g.136133009del , CM000671.1:g.136133009del GRCh37
NC_000009.10:g.135122830del NCBI36
NG_006669.1:g.20049del
NG_006669.2:g.22597del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-76del
ENST00000647353.1:n.54-6466del
ENST00000651471.1:n.329+424del
ENST00000679909.1:c.28+17544del ENSP00000506089.1:n.28+17544del
ENST00000453660.3:n.252-76del
ENST00000538324.2:c.240-76del ENSP00000483018.1:n.240-76del
ENST00000611156.4:c.240-76del ENSP00000483265.1:n.240-76del
NM_020469.2:c.240-76del NP_065202.2:n.240-76del
NM_020469.3:c.240-76del NP_065202.2:n.240-76del
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