Canonical Allele Identifier: CA1882579747
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255880C= , CM000671.2:g.133255880C= GRCh38
NC_000009.11:g.136131267C= , CM000671.1:g.136131267C= GRCh37
NC_000009.10:g.135121088C= NCBI36
NG_006669.1:g.21788G=
NG_006669.2:g.24336G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.880G=
ENST00000647353.1:n.54-4728G=
ENST00000679909.1:c.28+19282G= ENSP00000506089.1:n.28+19282G=
ENST00000453660.3:n.862G=
ENST00000538324.2:c.848G= ENSP00000483018.1:p.Cys283=
ENST00000611156.4:c.848G= ENSP00000483265.1:p.Cys283=
NM_020469.2:c.851G= NP_065202.2:p.Cys284=
NM_020469.3:c.851G= NP_065202.2:p.Cys284=