Canonical Allele Identifier: CA365337994
Gene: FOXO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2380243
ClinVar RCV Id: RCV004218757
dbSNP Id: rs1344931063
gnomAD v2: 6-108882746-C-T
gnomAD v3: 6-108561543-C-T
gnomAD v4: 6-108561543-C-T
MyVariant Identifiers: chr6:g.108882746C>T (hg19) chr6:g.108561543C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561543C>T , CM000668.2:g.108561543C>T GRCh38
NC_000006.11:g.108882746C>T , CM000668.1:g.108882746C>T GRCh37
NC_000006.10:g.108989439C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.335C>T MANE Select ENSP00000385824.1:p.Pro112Leu
ENST00000343882.10:c.335C>T ENSP00000339527.6:p.Pro112Leu
ENST00000406360.1:c.335C>T ENSP00000385824.1:p.Pro112Leu
NM_001455.3:c.335C>T NP_001446.1:p.Pro112Leu
NM_201559.2:c.335C>T NP_963853.1:p.Pro112Leu
NM_001455.4:c.335C>T MANE Select NP_001446.1:p.Pro112Leu
NM_201559.3:c.335C>T NP_963853.1:p.Pro112Leu
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