Canonical Allele Identifier: CA12435945
Gene: FOXO3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2764264

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108613258C>T , CM000668.2:g.108613258C>T GRCh38
NC_000006.11:g.108934461C>T , CM000668.1:g.108934461C>T GRCh37
NC_000006.10:g.109041154C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001455.3:c.622-50197C>T VV NP_001446.1:p.=
NM_201559.2:c.622-50197C>T VV NP_963853.1:p.=
XM_005266867.3:c.-63-26235C>T XP_005266924.1:p.=
XM_011535626.1:c.121-50197C>T XP_011533928.1:p.=
XM_011535627.1:c.69+26622C>T XP_011533929.1:p.=
XM_011535628.1:c.-40+23443C>T XP_011533930.1:p.=
XM_005266867.4:c.-63-26235C>T XP_005266924.1:p.=
XM_011535626.2:c.121-50197C>T XP_011533928.1:p.=
XM_011535628.3:c.-40+23443C>T XP_011533930.1:p.=
XM_017010585.1:c.-63-26235C>T XP_016866074.1:p.=
XM_017010586.1:c.-40+43516C>T XP_016866075.1:p.=
NM_001455.4:c.622-50197C>T VV MANE Preferred NP_001446.1:p.=
ENST00000343882.10:c.622-50197C>T ENSP00000339527.6:p.=
ENST00000406360.1:c.622-50197C>T ENSP00000385824.1:p.=