Canonical Allele Identifier: CA1882579866
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255920_133255921delinsCG , CM000671.2:g.133255920_133255921delinsCG GRCh38
NC_000009.11:g.136131307_136131308delinsCG , CM000671.1:g.136131307_136131308delinsCG GRCh37
NC_000009.10:g.135121128_135121129delinsCG NCBI36
NG_006669.1:g.21747_21748delinsCG
NG_006669.2:g.24295_24296delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.839_840delinsCG
ENST00000647353.1:n.54-4769_54-4768delinsCG
ENST00000679909.1:c.28+19241_28+19242delinsCG ENSP00000506089.1:n.28+19241_28+19242delinsCG
ENST00000453660.3:n.821_822delinsCG
ENST00000538324.2:c.807_808delinsCG ENSP00000483018.1:p.Phe269=
ENST00000611156.4:c.807_808delinsCG ENSP00000483265.1:p.Phe269=
NM_020469.2:c.810_811delinsCG NP_065202.2:p.Phe270=
NM_020469.3:c.810_811delinsCG NP_065202.2:p.Phe270=