Canonical Allele Identifier: CA365338752
Gene: FOXO3 HGNC NCBI

Linked Data

gnomAD v4: 6-108561753-A-G
MyVariant Identifiers: chr6:g.108882956A>G (hg19) chr6:g.108561753A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561753A>G , CM000668.2:g.108561753A>G GRCh38
NC_000006.11:g.108882956A>G , CM000668.1:g.108882956A>G GRCh37
NC_000006.10:g.108989649A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.545A>G MANE Select ENSP00000385824.1:p.Gln182Arg
ENST00000343882.10:c.545A>G ENSP00000339527.6:p.Gln182Arg
ENST00000406360.1:c.545A>G ENSP00000385824.1:p.Gln182Arg
NM_001455.3:c.545A>G NP_001446.1:p.Gln182Arg
NM_201559.2:c.545A>G NP_963853.1:p.Gln182Arg
XM_005266867.3:c.-140A>G XP_005266924.1:n.-140A>G
NM_001455.4:c.545A>G MANE Select NP_001446.1:p.Gln182Arg
NM_201559.3:c.545A>G NP_963853.1:p.Gln182Arg
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