Canonical Allele Identifier: CA365338865
Gene: FOXO3 HGNC NCBI

Linked Data

dbSNP Id: rs1775799342

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561800G>A , CM000668.2:g.108561800G>A GRCh38
NC_000006.11:g.108883003G>A , CM000668.1:g.108883003G>A GRCh37
NC_000006.10:g.108989696G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.592G>A MANE Select ENSP00000385824.1:p.Gly198Ser
ENST00000343882.10:c.592G>A ENSP00000339527.6:p.Gly198Ser
ENST00000406360.1:c.592G>A ENSP00000385824.1:p.Gly198Ser
NM_001455.3:c.592G>A NP_001446.1:p.Gly198Ser
NM_201559.2:c.592G>A NP_963853.1:p.Gly198Ser
XM_005266867.3:c.-93G>A XP_005266924.1:n.-93G>A
XM_005266867.4:c.-93G>A XP_005266924.1:n.-93G>A
NM_001455.4:c.592G>A MANE Select NP_001446.1:p.Gly198Ser
NM_201559.3:c.592G>A NP_963853.1:p.Gly198Ser