Canonical Allele Identifier: CA3949251
Gene: FOXO3 HGNC NCBI

Linked Data

dbSNP Id: rs369304108

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561773C>T , CM000668.2:g.108561773C>T GRCh38
NC_000006.11:g.108882976C>T , CM000668.1:g.108882976C>T GRCh37
NC_000006.10:g.108989669C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.565C>T MANE Select ENSP00000385824.1:p.Arg189Cys
ENST00000343882.10:c.565C>T ENSP00000339527.6:p.Arg189Cys
ENST00000406360.1:c.565C>T ENSP00000385824.1:p.Arg189Cys
NM_001455.3:c.565C>T NP_001446.1:p.Arg189Cys
NM_201559.2:c.565C>T NP_963853.1:p.Arg189Cys
XM_005266867.3:c.-120C>T XP_005266924.1:n.-120C>T
XM_005266867.4:c.-120C>T XP_005266924.1:n.-120C>T
NM_001455.4:c.565C>T MANE Select NP_001446.1:p.Arg189Cys
NM_201559.3:c.565C>T NP_963853.1:p.Arg189Cys