Canonical Allele Identifier: CA365337969
Gene: FOXO3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561530C>T , CM000668.2:g.108561530C>T GRCh38
NC_000006.11:g.108882733C>T , CM000668.1:g.108882733C>T GRCh37
NC_000006.10:g.108989426C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.322C>T MANE Select ENSP00000385824.1:p.Pro108Ser
ENST00000343882.10:c.322C>T ENSP00000339527.6:p.Pro108Ser
ENST00000406360.1:c.322C>T ENSP00000385824.1:p.Pro108Ser
NM_001455.3:c.322C>T NP_001446.1:p.Pro108Ser
NM_201559.2:c.322C>T NP_963853.1:p.Pro108Ser
NM_001455.4:c.322C>T MANE Select NP_001446.1:p.Pro108Ser
NM_201559.3:c.322C>T NP_963853.1:p.Pro108Ser