Canonical Allele Identifier: CA2692330565
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257506del , CM000671.2:g.133257506del GRCh38
NC_000009.11:g.136132893del , CM000671.1:g.136132893del GRCh37
NC_000009.10:g.135122714del NCBI36
NG_006669.1:g.20164del
NG_006669.2:g.22712del

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.308del
ENST00000647353.1:n.54-6352del
ENST00000651471.1:n.329+538del
ENST00000679909.1:c.28+17658del ENSP00000506089.1:n.28+17658del
ENST00000453660.3:n.290del
ENST00000538324.2:c.276del ENSP00000483018.1:p.Ile93LeufsTer25
ENST00000611156.4:c.276del ENSP00000483265.1:p.Ile93LeufsTer25
NM_020469.2:c.279del NP_065202.2:p.Ile94LeufsTer25
NM_020469.3:c.279del NP_065202.2:p.Ile94LeufsTer25