Canonical Allele Identifier: CA913819630
Gene: FOXO1 HGNC NCBI

Linked Data

dbSNP Id: rs1566075362
gnomAD v2: 13-41186418-C-T
gnomAD v3: 13-40612281-C-T
gnomAD v4: 13-40612281-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40612281C>T , CM000675.2:g.40612281C>T GRCh38
NC_000013.10:g.41186418C>T , CM000675.1:g.41186418C>T GRCh37
NC_000013.9:g.40084418C>T NCBI36
NG_023244.1:g.59317G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379561.6:c.631-51421G>A MANE Select ENSP00000368880.4:n.631-51421G>A
ENST00000655267.1:n.334-49519G>A
ENST00000660760.1:n.397+20866G>A
ENST00000379561.5:c.631-51421G>A ENSP00000368880.4:n.631-51421G>A
NM_002015.3:c.631-51421G>A NP_002006.2:n.631-51421G>A
XM_011535008.1:c.87+1869G>A XP_011533310.1:n.87+1869G>A
XR_941536.1:n.1226+33058G>A
XM_011535008.2:c.87+1869G>A XP_011533310.1:n.87+1869G>A
NM_002015.4:c.631-51421G>A MANE Select NP_002006.2:n.631-51421G>A
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