Canonical Allele Identifier: CA365338658
Gene: FOXO3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.108882913C>A (hg19) chr6:g.108561710C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561710C>A , CM000668.2:g.108561710C>A GRCh38
NC_000006.11:g.108882913C>A , CM000668.1:g.108882913C>A GRCh37
NC_000006.10:g.108989606C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000406360.2:c.502C>A MANE Select ENSP00000385824.1:p.Arg168Ser
ENST00000343882.10:c.502C>A ENSP00000339527.6:p.Arg168Ser
ENST00000406360.1:c.502C>A ENSP00000385824.1:p.Arg168Ser
NM_001455.3:c.502C>A NP_001446.1:p.Arg168Ser
NM_201559.2:c.502C>A NP_963853.1:p.Arg168Ser
NM_001455.4:c.502C>A MANE Select NP_001446.1:p.Arg168Ser
NM_201559.3:c.502C>A NP_963853.1:p.Arg168Ser
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