Canonical Allele Identifier: CA365338594
Gene: FOXO3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561679G>T , CM000668.2:g.108561679G>T GRCh38
NC_000006.11:g.108882882G>T , CM000668.1:g.108882882G>T GRCh37
NC_000006.10:g.108989575G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.471G>T MANE Select ENSP00000385824.1:p.Trp157Cys
ENST00000343882.10:c.471G>T ENSP00000339527.6:p.Trp157Cys
ENST00000406360.1:c.471G>T ENSP00000385824.1:p.Trp157Cys
NM_001455.3:c.471G>T NP_001446.1:p.Trp157Cys
NM_201559.2:c.471G>T NP_963853.1:p.Trp157Cys
NM_001455.4:c.471G>T MANE Select NP_001446.1:p.Trp157Cys
NM_201559.3:c.471G>T NP_963853.1:p.Trp157Cys