Canonical Allele Identifier: CA2954284205
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255991del , CM000671.2:g.133255991del GRCh38
NC_000009.11:g.136131378del , CM000671.1:g.136131378del GRCh37
NC_000009.10:g.135121199del NCBI36
NG_006669.1:g.21677del
NG_006669.2:g.24225del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.769del
ENST00000647353.1:n.54-4839del
ENST00000679909.1:c.28+19171del ENSP00000506089.1:n.28+19171del
ENST00000453660.3:n.751del
ENST00000538324.2:c.737del ENSP00000483018.1:p.Glu246GlyfsTer?
ENST00000611156.4:c.737del ENSP00000483265.1:p.Glu246GlyfsTer?
NM_020469.2:c.740del NP_065202.2:p.Glu247GlyfsTer?
NM_020469.3:c.740del NP_065202.2:p.Glu247GlyfsTer?