Canonical Allele Identifier: CA2521371700
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255377del , CM000671.2:g.133255377del GRCh38
NC_000009.11:g.136130764del , CM000671.1:g.136130764del GRCh37
NC_000009.10:g.135120585del NCBI36
NG_006669.1:g.22294del
NG_006669.2:g.24842del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1386del
ENST00000647353.1:n.54-4222del
ENST00000679909.1:c.28+19788del ENSP00000506089.1:n.28+19788del
ENST00000453660.3:n.1368del
ENST00000611156.4:c.*292del ENSP00000483265.1:n.*292del
NM_020469.2:c.*292del NP_065202.2:n.*292del
NM_020469.3:c.*292del NP_065202.2:n.*292del