Canonical Allele Identifier: CA2538211491
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255297del , CM000671.2:g.133255297del GRCh38
NC_000009.11:g.136130684del , CM000671.1:g.136130684del GRCh37
NC_000009.10:g.135120505del NCBI36
NG_006669.1:g.22372del
NG_006669.2:g.24920del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1464del
ENST00000647353.1:n.54-4144del
ENST00000679909.1:c.28+19866del ENSP00000506089.1:n.28+19866del
ENST00000453660.3:n.1446del
ENST00000611156.4:c.*370del ENSP00000483265.1:n.*370del
NM_020469.2:c.*370del NP_065202.2:n.*370del
NM_020469.3:c.*370del NP_065202.2:n.*370del