Canonical Allele Identifier: CA365338799
Gene: FOXO3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561771T>A , CM000668.2:g.108561771T>A GRCh38
NC_000006.11:g.108882974T>A , CM000668.1:g.108882974T>A GRCh37
NC_000006.10:g.108989667T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.563T>A MANE Select ENSP00000385824.1:p.Val188Glu
ENST00000343882.10:c.563T>A ENSP00000339527.6:p.Val188Glu
ENST00000406360.1:c.563T>A ENSP00000385824.1:p.Val188Glu
NM_001455.3:c.563T>A NP_001446.1:p.Val188Glu
NM_201559.2:c.563T>A NP_963853.1:p.Val188Glu
XM_005266867.3:c.-122T>A XP_005266924.1:n.-122T>A
XM_005266867.4:c.-122T>A XP_005266924.1:n.-122T>A
NM_001455.4:c.563T>A MANE Select NP_001446.1:p.Val188Glu
NM_201559.3:c.563T>A NP_963853.1:p.Val188Glu