Canonical Allele Identifier: CA365338641
Gene: FOXO3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561701C>G , CM000668.2:g.108561701C>G GRCh38
NC_000006.11:g.108882904C>G , CM000668.1:g.108882904C>G GRCh37
NC_000006.10:g.108989597C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.493C>G MANE Select ENSP00000385824.1:p.Leu165Val
ENST00000343882.10:c.493C>G ENSP00000339527.6:p.Leu165Val
ENST00000406360.1:c.493C>G ENSP00000385824.1:p.Leu165Val
NM_001455.3:c.493C>G NP_001446.1:p.Leu165Val
NM_201559.2:c.493C>G NP_963853.1:p.Leu165Val
NM_001455.4:c.493C>G MANE Select NP_001446.1:p.Leu165Val
NM_201559.3:c.493C>G NP_963853.1:p.Leu165Val