Canonical Allele Identifier: CA365338851
Gene: FOXO3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561794G>T , CM000668.2:g.108561794G>T GRCh38
NC_000006.11:g.108882997G>T , CM000668.1:g.108882997G>T GRCh37
NC_000006.10:g.108989690G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.586G>T MANE Select ENSP00000385824.1:p.Asp196Tyr
ENST00000343882.10:c.586G>T ENSP00000339527.6:p.Asp196Tyr
ENST00000406360.1:c.586G>T ENSP00000385824.1:p.Asp196Tyr
NM_001455.3:c.586G>T NP_001446.1:p.Asp196Tyr
NM_201559.2:c.586G>T NP_963853.1:p.Asp196Tyr
XM_005266867.3:c.-99G>T XP_005266924.1:n.-99G>T
XM_005266867.4:c.-99G>T XP_005266924.1:n.-99G>T
NM_001455.4:c.586G>T MANE Select NP_001446.1:p.Asp196Tyr
NM_201559.3:c.586G>T NP_963853.1:p.Asp196Tyr