Canonical Allele Identifier: CA2727959366
Gene: FOXO1 HGNC NCBI

Linked Data

dbSNP Id: rs2137926061

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644132C>T , CM000675.2:g.40644132C>T GRCh38
NC_000013.10:g.41218269C>T , CM000675.1:g.41218269C>T GRCh37
NC_000013.9:g.40116269C>T NCBI36
NG_023244.1:g.27466G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379561.6:c.630+21451G>A MANE Select ENSP00000368880.4:n.630+21451G>A
ENST00000655267.1:n.333+21451G>A
ENST00000660760.1:n.296-10884G>A
ENST00000379561.5:c.630+21451G>A ENSP00000368880.4:n.630+21451G>A
NM_002015.3:c.630+21451G>A NP_002006.2:n.630+21451G>A
XR_941536.1:n.1226+1207G>A
NM_002015.4:c.630+21451G>A MANE Select NP_002006.2:n.630+21451G>A