Canonical Allele Identifier: CA1654338021
Gene: FOXO3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561536T= , CM000668.2:g.108561536T= GRCh38
NC_000006.11:g.108882739T= , CM000668.1:g.108882739T= GRCh37
NC_000006.10:g.108989432T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.328T= MANE Select ENSP00000385824.1:p.Ser110=
ENST00000343882.10:c.328T= ENSP00000339527.6:p.Ser110=
ENST00000406360.1:c.328T= ENSP00000385824.1:p.Ser110=
NM_001455.3:c.328T= NP_001446.1:p.Ser110=
NM_201559.2:c.328T= NP_963853.1:p.Ser110=
NM_001455.4:c.328T= MANE Select NP_001446.1:p.Ser110=
NM_201559.3:c.328T= NP_963853.1:p.Ser110=
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