Canonical Allele Identifier: CA2692330337
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255605_133255607del , CM000671.2:g.133255605_133255607del GRCh38
NC_000009.11:g.136130992_136130994del , CM000671.1:g.136130992_136130994del GRCh37
NC_000009.10:g.135120813_135120815del NCBI36
NG_006669.1:g.22062_22064del
NG_006669.2:g.24610_24612del

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.1154_1156del
ENST00000647353.1:n.54-4454_54-4452del
ENST00000679909.1:c.28+19556_28+19558del ENSP00000506089.1:n.28+19556_28+19558del
ENST00000453660.3:n.1136_1138del
ENST00000538324.2:c.1118_1120del ENSP00000483018.1:p.Phe373Ter
ENST00000611156.4:c.*60_*62del ENSP00000483265.1:n.*60_*62del
NM_020469.2:c.*60_*62del NP_065202.2:n.*60_*62del
NM_020469.3:c.*60_*62del NP_065202.2:n.*60_*62del