Canonical Allele Identifier: CA955234937
Gene: FOXO1 HGNC NCBI

Linked Data

dbSNP Id: rs1381713669
gnomAD v3: 13-40644571-T-C
gnomAD v4: 13-40644571-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644571T>C , CM000675.2:g.40644571T>C GRCh38
NC_000013.10:g.41218708T>C , CM000675.1:g.41218708T>C GRCh37
NC_000013.9:g.40116708T>C NCBI36
NG_023244.1:g.27027A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379561.6:c.630+21012A>G MANE Select ENSP00000368880.4:n.630+21012A>G
ENST00000655267.1:n.333+21012A>G
ENST00000660760.1:n.296-11323A>G
ENST00000379561.5:c.630+21012A>G ENSP00000368880.4:n.630+21012A>G
NM_002015.3:c.630+21012A>G NP_002006.2:n.630+21012A>G
XR_941536.1:n.1226+768A>G
NM_002015.4:c.630+21012A>G MANE Select NP_002006.2:n.630+21012A>G
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