Canonical Allele Identifier: CA365338785
Gene: FOXO3 HGNC NCBI

Linked Data

gnomAD v4: 6-108561766-G-A
MyVariant Identifiers: chr6:g.108882969G>A (hg19) chr6:g.108561766G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561766G>A , CM000668.2:g.108561766G>A GRCh38
NC_000006.11:g.108882969G>A , CM000668.1:g.108882969G>A GRCh37
NC_000006.10:g.108989662G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.558G>A MANE Select ENSP00000385824.1:p.Trp186Ter
ENST00000343882.10:c.558G>A ENSP00000339527.6:p.Trp186Ter
ENST00000406360.1:c.558G>A ENSP00000385824.1:p.Trp186Ter
NM_001455.3:c.558G>A NP_001446.1:p.Trp186Ter
NM_201559.2:c.558G>A NP_963853.1:p.Trp186Ter
XM_005266867.3:c.-127G>A XP_005266924.1:n.-127G>A
XM_005266867.4:c.-127G>A XP_005266924.1:n.-127G>A
NM_001455.4:c.558G>A MANE Select NP_001446.1:p.Trp186Ter
NM_201559.3:c.558G>A NP_963853.1:p.Trp186Ter
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