Canonical Allele Identifier: CA2692330357
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256071del , CM000671.2:g.133256071del GRCh38
NC_000009.11:g.136131458del , CM000671.1:g.136131458del GRCh37
NC_000009.10:g.135121279del NCBI36
NG_006669.1:g.21599del
NG_006669.2:g.24147del

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.691del
ENST00000647353.1:n.54-4917del
ENST00000679909.1:c.28+19093del ENSP00000506089.1:n.28+19093del
ENST00000453660.3:n.673del
ENST00000538324.2:c.659del ENSP00000483018.1:p.Gly220AlafsTer5
ENST00000611156.4:c.659del ENSP00000483265.1:p.Gly220AlafsTer5
NM_020469.2:c.662del NP_065202.2:p.Gly221AlafsTer5
NM_020469.3:c.662del NP_065202.2:p.Gly221AlafsTer5