Canonical Allele Identifier: CA248982954
Gene: FOXO1 HGNC NCBI

Linked Data

dbSNP Id: rs1023045355
gnomAD v2: 13-41218701-T-C
gnomAD v3: 13-40644564-T-C
gnomAD v4: 13-40644564-T-C
MyVariant Identifiers: chr13:g.41218701T>C (hg19) chr13:g.40644564T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644564T>C , CM000675.2:g.40644564T>C GRCh38
NC_000013.10:g.41218701T>C , CM000675.1:g.41218701T>C GRCh37
NC_000013.9:g.40116701T>C NCBI36
NG_023244.1:g.27034A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379561.6:c.630+21019A>G MANE Select ENSP00000368880.4:n.630+21019A>G
ENST00000655267.1:n.333+21019A>G
ENST00000660760.1:n.296-11316A>G
ENST00000379561.5:c.630+21019A>G ENSP00000368880.4:n.630+21019A>G
NM_002015.3:c.630+21019A>G NP_002006.2:n.630+21019A>G
XR_941536.1:n.1226+775A>G
NM_002015.4:c.630+21019A>G MANE Select NP_002006.2:n.630+21019A>G
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