Canonical Allele Identifier: CA1882579744
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255879G= , CM000671.2:g.133255879G= GRCh38
NC_000009.11:g.136131266G= , CM000671.1:g.136131266G= GRCh37
NC_000009.10:g.135121087G= NCBI36
NG_006669.1:g.21789C=
NG_006669.2:g.24337C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.881C=
ENST00000647353.1:n.54-4727C=
ENST00000679909.1:c.28+19283C= ENSP00000506089.1:n.28+19283C=
ENST00000453660.3:n.863C=
ENST00000538324.2:c.849C= ENSP00000483018.1:p.Cys283=
ENST00000611156.4:c.849C= ENSP00000483265.1:p.Cys283=
NM_020469.2:c.852C= NP_065202.2:p.Cys284=
NM_020469.3:c.852C= NP_065202.2:p.Cys284=