Canonical Allele Identifier: CA365338762
Gene: FOXO3 HGNC NCBI

Linked Data

gnomAD v4: 6-108561757-C-G
MyVariant Identifiers: chr6:g.108882960C>G (hg19) chr6:g.108561757C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561757C>G , CM000668.2:g.108561757C>G GRCh38
NC_000006.11:g.108882960C>G , CM000668.1:g.108882960C>G GRCh37
NC_000006.10:g.108989653C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.549C>G MANE Select ENSP00000385824.1:p.Ile183Met
ENST00000343882.10:c.549C>G ENSP00000339527.6:p.Ile183Met
ENST00000406360.1:c.549C>G ENSP00000385824.1:p.Ile183Met
NM_001455.3:c.549C>G NP_001446.1:p.Ile183Met
NM_201559.2:c.549C>G NP_963853.1:p.Ile183Met
XM_005266867.3:c.-136C>G XP_005266924.1:n.-136C>G
NM_001455.4:c.549C>G MANE Select NP_001446.1:p.Ile183Met
NM_201559.3:c.549C>G NP_963853.1:p.Ile183Met
Search 100 bp 5'
Search 100 bp 3'