Canonical Allele Identifier: CA1882580774
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256249_133256250delinsCG , CM000671.2:g.133256249_133256250delinsCG GRCh38
NC_000009.11:g.136131636_136131637delinsCG , CM000671.1:g.136131636_136131637delinsCG GRCh37
NC_000009.10:g.135121457_135121458delinsCG NCBI36
NG_006669.1:g.21418_21419delinsCG
NG_006669.2:g.23966_23967delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.510_511delinsCG
ENST00000647353.1:n.54-5098_54-5097delinsCG
ENST00000651471.1:n.436_437delinsCG
ENST00000679909.1:c.28+18912_28+18913delinsCG ENSP00000506089.1:n.28+18912_28+18913delinsCG
ENST00000453660.3:n.492_493delinsCG
ENST00000538324.2:c.478_479delinsCG ENSP00000483018.1:p.Arg160=
ENST00000611156.4:c.478_479delinsCG ENSP00000483265.1:p.Arg160=
NM_020469.2:c.481_482delinsCG NP_065202.2:p.Arg161=
NM_020469.3:c.481_482delinsCG NP_065202.2:p.Arg161=