Canonical Allele Identifier: CA1654338362
Gene: FOXO3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561697G= , CM000668.2:g.108561697G= GRCh38
NC_000006.11:g.108882900G= , CM000668.1:g.108882900G= GRCh37
NC_000006.10:g.108989593G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.489G= MANE Select ENSP00000385824.1:p.Ala163=
ENST00000343882.10:c.489G= ENSP00000339527.6:p.Ala163=
ENST00000406360.1:c.489G= ENSP00000385824.1:p.Ala163=
NM_001455.3:c.489G= NP_001446.1:p.Ala163=
NM_201559.2:c.489G= NP_963853.1:p.Ala163=
NM_001455.4:c.489G= MANE Select NP_001446.1:p.Ala163=
NM_201559.3:c.489G= NP_963853.1:p.Ala163=