Canonical Allele Identifier: CA451920678
Gene: FOXO3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.108883005C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561802C>A , CM000668.2:g.108561802C>A GRCh38
NC_000006.11:g.108883005C>A , CM000668.1:g.108883005C>A GRCh37
NC_000006.10:g.108989698C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000406360.2:c.594C>A MANE Select ENSP00000385824.1:p.Gly198=
ENST00000343882.10:c.594C>A ENSP00000339527.6:p.Gly198=
ENST00000406360.1:c.594C>A ENSP00000385824.1:p.Gly198=
NM_001455.3:c.594C>A NP_001446.1:p.Gly198=
NM_201559.2:c.594C>A NP_963853.1:p.Gly198=
XM_005266867.3:c.-91C>A XP_005266924.1:n.-91C>A
XM_005266867.4:c.-91C>A XP_005266924.1:n.-91C>A
NM_001455.4:c.594C>A MANE Select NP_001446.1:p.Gly198=
NM_201559.3:c.594C>A NP_963853.1:p.Gly198=