Canonical Allele Identifier: CA365338844
Gene: FOXO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 438763
ClinVar RCV Id: RCV000505594
dbSNP Id: rs1554209779

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561791A>T , CM000668.2:g.108561791A>T GRCh38
NC_000006.11:g.108882994A>T , CM000668.1:g.108882994A>T GRCh37
NC_000006.10:g.108989687A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000406360.2:c.583A>T MANE Select ENSP00000385824.1:p.Lys195Ter
ENST00000343882.10:c.583A>T ENSP00000339527.6:p.Lys195Ter
ENST00000406360.1:c.583A>T ENSP00000385824.1:p.Lys195Ter
NM_001455.3:c.583A>T NP_001446.1:p.Lys195Ter
NM_201559.2:c.583A>T NP_963853.1:p.Lys195Ter
XM_005266867.3:c.-102A>T XP_005266924.1:n.-102A>T
XM_005266867.4:c.-102A>T XP_005266924.1:n.-102A>T
NM_001455.4:c.583A>T MANE Select NP_001446.1:p.Lys195Ter
NM_201559.3:c.583A>T NP_963853.1:p.Lys195Ter