Canonical Allele Identifier: CA365338545
Gene: FOXO3 HGNC NCBI

Linked Data

dbSNP Id: rs1562224143
MyVariant Identifiers: chr6:g.108882859T>G (hg19) chr6:g.108561656T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561656T>G , CM000668.2:g.108561656T>G GRCh38
NC_000006.11:g.108882859T>G , CM000668.1:g.108882859T>G GRCh37
NC_000006.10:g.108989552T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.448T>G MANE Select ENSP00000385824.1:p.Cys150Gly
ENST00000343882.10:c.448T>G ENSP00000339527.6:p.Cys150Gly
ENST00000406360.1:c.448T>G ENSP00000385824.1:p.Cys150Gly
NM_001455.3:c.448T>G NP_001446.1:p.Cys150Gly
NM_201559.2:c.448T>G NP_963853.1:p.Cys150Gly
NM_001455.4:c.448T>G MANE Select NP_001446.1:p.Cys150Gly
NM_201559.3:c.448T>G NP_963853.1:p.Cys150Gly
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