Canonical Allele Identifier: CA955234776
Gene: FOXO1 HGNC NCBI

Linked Data

dbSNP Id: rs1877441056
gnomAD v3: 13-40644169-T-C
gnomAD v4: 13-40644169-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644169T>C , CM000675.2:g.40644169T>C GRCh38
NC_000013.10:g.41218306T>C , CM000675.1:g.41218306T>C GRCh37
NC_000013.9:g.40116306T>C NCBI36
NG_023244.1:g.27429A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000379561.6:c.630+21414A>G MANE Select ENSP00000368880.4:n.630+21414A>G
ENST00000655267.1:n.333+21414A>G
ENST00000660760.1:n.296-10921A>G
ENST00000379561.5:c.630+21414A>G ENSP00000368880.4:n.630+21414A>G
NM_002015.3:c.630+21414A>G NP_002006.2:n.630+21414A>G
XR_941536.1:n.1226+1170A>G
NM_002015.4:c.630+21414A>G MANE Select NP_002006.2:n.630+21414A>G
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