Canonical Allele Identifier: CA2507899455
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255409del , CM000671.2:g.133255409del GRCh38
NC_000009.11:g.136130796del , CM000671.1:g.136130796del GRCh37
NC_000009.10:g.135120617del NCBI36
NG_006669.1:g.22259del
NG_006669.2:g.24807del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1351del
ENST00000647353.1:n.54-4257del
ENST00000679909.1:c.28+19753del ENSP00000506089.1:n.28+19753del
ENST00000453660.3:n.1333del
ENST00000611156.4:c.*257del ENSP00000483265.1:n.*257del
NM_020469.2:c.*257del NP_065202.2:n.*257del
NM_020469.3:c.*257del NP_065202.2:n.*257del