Canonical Allele Identifier: CA1129725038
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274142_133274144del , CM000671.2:g.133274142_133274144del GRCh38
NC_000009.11:g.136149558_136149560del , CM000671.1:g.136149558_136149560del GRCh37
NC_000009.10:g.135139379_135139381del NCBI36
NG_006669.1:g.3491_3493del
NG_006669.2:g.6071_6073del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.58+1018_58+1020del
ENST00000647353.1:n.53+1018_53+1020del
ENST00000651471.1:n.63+1818_63+1820del
ENST00000679909.1:c.28+1018_28+1020del ENSP00000506089.1:n.28+1018_28+1020del
ENST00000453660.3:n.40+1018_40+1020del
ENST00000538324.2:c.28+1018_28+1020del ENSP00000483018.1:n.28+1018_28+1020del
ENST00000611156.4:c.28+1018_28+1020del ENSP00000483265.1:n.28+1018_28+1020del
NM_020469.2:c.28+1018_28+1020del NP_065202.2:n.28+1018_28+1020del
NM_020469.3:c.28+1018_28+1020del NP_065202.2:n.28+1018_28+1020del