Canonical Allele Identifier: CA12203848
Gene: FOXO3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1935952

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108677702G>C , CM000668.2:g.108677702G>C GRCh38
NC_000006.11:g.108998905G>C , CM000668.1:g.108998905G>C GRCh37
NC_000006.10:g.109105598G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001455.3:c.*35-2125G>C VV NP_001446.1:p.=
NM_201559.2:c.*35-2125G>C VV NP_963853.1:p.=
XM_005266867.3:c.*35-2125G>C XP_005266924.1:p.=
XM_005266868.2:c.*35-2125G>C XP_005266925.1:p.=
XM_011535626.1:c.*35-2125G>C XP_011533928.1:p.=
XM_011535627.1:c.*35-2125G>C XP_011533929.1:p.=
XM_011535628.1:c.*35-2125G>C XP_011533930.1:p.=
XM_011535629.1:c.*35-2125G>C XP_011533931.1:p.=
XM_005266867.4:c.*35-2125G>C XP_005266924.1:p.=
XM_005266868.3:c.*35-2125G>C XP_005266925.1:p.=
XM_011535626.2:c.*35-2125G>C XP_011533928.1:p.=
XM_011535628.3:c.*35-2125G>C XP_011533930.1:p.=
XM_011535629.2:c.*35-2125G>C XP_011533931.1:p.=
XM_017010585.1:c.*35-2125G>C XP_016866074.1:p.=
XM_017010586.1:c.*35-2125G>C XP_016866075.1:p.=
NM_001455.4:c.*35-2125G>C VV MANE Preferred NP_001446.1:p.=
ENST00000343882.10:c.*35-2125G>C ENSP00000339527.6:p.=
ENST00000406360.1:c.*35-2125G>C ENSP00000385824.1:p.=
ENST00000540898.1:c.*35-2125G>C ENSP00000446316.1:p.=