Canonical Allele Identifier: CA365338626
Gene: FOXO3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561694C>A , CM000668.2:g.108561694C>A GRCh38
NC_000006.11:g.108882897C>A , CM000668.1:g.108882897C>A GRCh37
NC_000006.10:g.108989590C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000406360.2:c.486C>A MANE Select ENSP00000385824.1:p.Tyr162Ter
ENST00000343882.10:c.486C>A ENSP00000339527.6:p.Tyr162Ter
ENST00000406360.1:c.486C>A ENSP00000385824.1:p.Tyr162Ter
NM_001455.3:c.486C>A NP_001446.1:p.Tyr162Ter
NM_201559.2:c.486C>A NP_963853.1:p.Tyr162Ter
NM_001455.4:c.486C>A MANE Select NP_001446.1:p.Tyr162Ter
NM_201559.3:c.486C>A NP_963853.1:p.Tyr162Ter