Canonical Allele Identifier: CA1882579348
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255721C= , CM000671.2:g.133255721C= GRCh38
NC_000009.11:g.136131108C= , CM000671.1:g.136131108C= GRCh37
NC_000009.10:g.135120929C= NCBI36
NG_006669.1:g.21947G=
NG_006669.2:g.24495G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.1039G=
ENST00000647353.1:n.54-4569G=
ENST00000679909.1:c.28+19441G= ENSP00000506089.1:n.28+19441G=
ENST00000453660.3:n.1021G=
ENST00000538324.2:c.1007G= ENSP00000483018.1:p.Arg336=
ENST00000611156.4:c.1007G= ENSP00000483265.1:p.Arg336=
NM_020469.2:c.1010G= NP_065202.2:p.Arg337=
NM_020469.3:c.1010G= NP_065202.2:p.Arg337=