Canonical Allele Identifier: CA145712192
Gene: FOXO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2494092
ClinVar RCV Id: RCV004280848
dbSNP Id: rs944210246
gnomAD v3: 6-108561564-T-A
gnomAD v4: 6-108561564-T-A
MyVariant Identifiers: chr6:g.108882767T>A (hg19) chr6:g.108561564T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561564T>A , CM000668.2:g.108561564T>A GRCh38
NC_000006.11:g.108882767T>A , CM000668.1:g.108882767T>A GRCh37
NC_000006.10:g.108989460T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.356T>A MANE Select ENSP00000385824.1:p.Leu119Gln
ENST00000343882.10:c.356T>A ENSP00000339527.6:p.Leu119Gln
ENST00000406360.1:c.356T>A ENSP00000385824.1:p.Leu119Gln
NM_001455.3:c.356T>A NP_001446.1:p.Leu119Gln
NM_201559.2:c.356T>A NP_963853.1:p.Leu119Gln
NM_001455.4:c.356T>A MANE Select NP_001446.1:p.Leu119Gln
NM_201559.3:c.356T>A NP_963853.1:p.Leu119Gln
Search 100 bp 5'
Search 100 bp 3'