Canonical Allele Identifier: CA145712203
Gene: FOXO3 HGNC NCBI

Linked Data

dbSNP Id: rs567562629

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561798A>G , CM000668.2:g.108561798A>G GRCh38
NC_000006.11:g.108883001A>G , CM000668.1:g.108883001A>G GRCh37
NC_000006.10:g.108989694A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000406360.2:c.590A>G MANE Select ENSP00000385824.1:p.Lys197Arg
ENST00000343882.10:c.590A>G ENSP00000339527.6:p.Lys197Arg
ENST00000406360.1:c.590A>G ENSP00000385824.1:p.Lys197Arg
NM_001455.3:c.590A>G NP_001446.1:p.Lys197Arg
NM_201559.2:c.590A>G NP_963853.1:p.Lys197Arg
XM_005266867.3:c.-95A>G XP_005266924.1:n.-95A>G
XM_005266867.4:c.-95A>G XP_005266924.1:n.-95A>G
NM_001455.4:c.590A>G MANE Select NP_001446.1:p.Lys197Arg
NM_201559.3:c.590A>G NP_963853.1:p.Lys197Arg