Canonical Allele Identifier: CA3949218
Gene: FOXO3 HGNC NCBI

Linked Data

dbSNP Id: rs776502822

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561601A>C , CM000668.2:g.108561601A>C GRCh38
NC_000006.11:g.108882804A>C , CM000668.1:g.108882804A>C GRCh37
NC_000006.10:g.108989497A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.393A>C MANE Select ENSP00000385824.1:p.Gln131His
ENST00000343882.10:c.393A>C ENSP00000339527.6:p.Gln131His
ENST00000406360.1:c.393A>C ENSP00000385824.1:p.Gln131His
NM_001455.3:c.393A>C NP_001446.1:p.Gln131His
NM_201559.2:c.393A>C NP_963853.1:p.Gln131His
NM_001455.4:c.393A>C MANE Select NP_001446.1:p.Gln131His
NM_201559.3:c.393A>C NP_963853.1:p.Gln131His