Canonical Allele Identifier: CA1882580291
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256081C= , CM000671.2:g.133256081C= GRCh38
NC_000009.11:g.136131468C= , CM000671.1:g.136131468C= GRCh37
NC_000009.10:g.135121289C= NCBI36
NG_006669.1:g.21587G=
NG_006669.2:g.24135G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.679G=
ENST00000647353.1:n.54-4929G=
ENST00000679909.1:c.28+19081G= ENSP00000506089.1:n.28+19081G=
ENST00000453660.3:n.661G=
ENST00000538324.2:c.647G= ENSP00000483018.1:p.Arg216=
ENST00000611156.4:c.647G= ENSP00000483265.1:p.Arg216=
NM_020469.2:c.650G= NP_065202.2:p.Arg217=
NM_020469.3:c.650G= NP_065202.2:p.Arg217=