Canonical Allele Identifier: CA1882580332
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256097_133256098delinsCG , CM000671.2:g.133256097_133256098delinsCG GRCh38
NC_000009.11:g.136131484_136131485delinsCG , CM000671.1:g.136131484_136131485delinsCG GRCh37
NC_000009.10:g.135121305_135121306delinsCG NCBI36
NG_006669.1:g.21570_21571delinsCG
NG_006669.2:g.24118_24119delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.662_663delinsCG
ENST00000647353.1:n.54-4946_54-4945delinsCG
ENST00000679909.1:c.28+19064_28+19065delinsCG ENSP00000506089.1:n.28+19064_28+19065deli...
ENST00000453660.3:n.644_645delinsCG
ENST00000538324.2:c.630_631delinsCG ENSP00000483018.1:p.Asp210=
ENST00000611156.4:c.630_631delinsCG ENSP00000483265.1:p.Asp210=
NM_020469.2:c.633_634delinsCG NP_065202.2:p.Asp211=
NM_020469.3:c.633_634delinsCG NP_065202.2:p.Asp211=