Canonical Allele Identifier: CA3949225
Gene: FOXO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 770927
ClinVar RCV Id: RCV000950149
dbSNP Id: rs111556510

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561627C>T , CM000668.2:g.108561627C>T GRCh38
NC_000006.11:g.108882830C>T , CM000668.1:g.108882830C>T GRCh37
NC_000006.10:g.108989523C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.419C>T MANE Select ENSP00000385824.1:p.Ala140Val
ENST00000343882.10:c.419C>T ENSP00000339527.6:p.Ala140Val
ENST00000406360.1:c.419C>T ENSP00000385824.1:p.Ala140Val
NM_001455.3:c.419C>T NP_001446.1:p.Ala140Val
NM_201559.2:c.419C>T NP_963853.1:p.Ala140Val
NM_001455.4:c.419C>T MANE Select NP_001446.1:p.Ala140Val
NM_201559.3:c.419C>T NP_963853.1:p.Ala140Val