Canonical Allele Identifier: CA451920521
Gene: FOXO3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.108882915C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561712C>A , CM000668.2:g.108561712C>A GRCh38
NC_000006.11:g.108882915C>A , CM000668.1:g.108882915C>A GRCh37
NC_000006.10:g.108989608C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.504C>A MANE Select ENSP00000385824.1:p.Arg168=
ENST00000343882.10:c.504C>A ENSP00000339527.6:p.Arg168=
ENST00000406360.1:c.504C>A ENSP00000385824.1:p.Arg168=
NM_001455.3:c.504C>A NP_001446.1:p.Arg168=
NM_201559.2:c.504C>A NP_963853.1:p.Arg168=
NM_001455.4:c.504C>A MANE Select NP_001446.1:p.Arg168=
NM_201559.3:c.504C>A NP_963853.1:p.Arg168=