Canonical Allele Identifier: CA591377548
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255176_133255387del , CM000671.2:g.133255176_133255387del GRCh38
NC_000009.11:g.136130563_136130774del , CM000671.1:g.136130563_136130774del GRCh37
NC_000009.10:g.135120384_135120595del NCBI36
NG_006669.2:g.24895_25106del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1439_1650del
ENST00000647353.1:n.54-4169_54-3958del
ENST00000679909.1:c.28+19841_28+20052del ENSP00000506089.1:n.28+19841_28+20052del
ENST00000453660.3:n.1421_1632del
NM_020469.3:c.*345_*556del NP_065202.2:n.*345_*556del