Canonical Allele Identifier: CA145712200
Gene: FOXO3 HGNC NCBI

Linked Data

dbSNP Id: rs1044892

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561695G>T , CM000668.2:g.108561695G>T GRCh38
NC_000006.11:g.108882898G>T , CM000668.1:g.108882898G>T GRCh37
NC_000006.10:g.108989591G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000406360.2:c.487G>T MANE Select ENSP00000385824.1:p.Ala163Ser
ENST00000343882.10:c.487G>T ENSP00000339527.6:p.Ala163Ser
ENST00000406360.1:c.487G>T ENSP00000385824.1:p.Ala163Ser
NM_001455.3:c.487G>T NP_001446.1:p.Ala163Ser
NM_201559.2:c.487G>T NP_963853.1:p.Ala163Ser
NM_001455.4:c.487G>T MANE Select NP_001446.1:p.Ala163Ser
NM_201559.3:c.487G>T NP_963853.1:p.Ala163Ser