Canonical Allele Identifier: CA2086517969
Gene: FOXO1 HGNC NCBI

Linked Data

dbSNP Id: rs1279483727

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644595A>C , CM000675.2:g.40644595A>C GRCh38
NC_000013.10:g.41218732A>C , CM000675.1:g.41218732A>C GRCh37
NC_000013.9:g.40116732A>C NCBI36
NG_023244.1:g.27003T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379561.6:c.630+20988T>G MANE Select ENSP00000368880.4:n.630+20988T>G
ENST00000655267.1:n.333+20988T>G
ENST00000660760.1:n.296-11347T>G
ENST00000379561.5:c.630+20988T>G ENSP00000368880.4:n.630+20988T>G
NM_002015.3:c.630+20988T>G NP_002006.2:n.630+20988T>G
XR_941536.1:n.1226+744T>G
NM_002015.4:c.630+20988T>G MANE Select NP_002006.2:n.630+20988T>G