Canonical Allele Identifier: CA365338800
Gene: FOXO3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.108882974T>C (hg19) chr6:g.108561771T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561771T>C , CM000668.2:g.108561771T>C GRCh38
NC_000006.11:g.108882974T>C , CM000668.1:g.108882974T>C GRCh37
NC_000006.10:g.108989667T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.563T>C MANE Select ENSP00000385824.1:p.Val188Ala
ENST00000343882.10:c.563T>C ENSP00000339527.6:p.Val188Ala
ENST00000406360.1:c.563T>C ENSP00000385824.1:p.Val188Ala
NM_001455.3:c.563T>C NP_001446.1:p.Val188Ala
NM_201559.2:c.563T>C NP_963853.1:p.Val188Ala
XM_005266867.3:c.-122T>C XP_005266924.1:n.-122T>C
XM_005266867.4:c.-122T>C XP_005266924.1:n.-122T>C
NM_001455.4:c.563T>C MANE Select NP_001446.1:p.Val188Ala
NM_201559.3:c.563T>C NP_963853.1:p.Val188Ala
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