Canonical Allele Identifier: CA1654338518
Gene: FOXO3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561772G= , CM000668.2:g.108561772G= GRCh38
NC_000006.11:g.108882975G= , CM000668.1:g.108882975G= GRCh37
NC_000006.10:g.108989668G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.564G= MANE Select ENSP00000385824.1:p.Val188=
ENST00000343882.10:c.564G= ENSP00000339527.6:p.Val188=
ENST00000406360.1:c.564G= ENSP00000385824.1:p.Val188=
NM_001455.3:c.564G= NP_001446.1:p.Val188=
NM_201559.2:c.564G= NP_963853.1:p.Val188=
XM_005266867.3:c.-121G= XP_005266924.1:n.-121G=
XM_005266867.4:c.-121G= XP_005266924.1:n.-121G=
NM_001455.4:c.564G= MANE Select NP_001446.1:p.Val188=
NM_201559.3:c.564G= NP_963853.1:p.Val188=