Canonical Allele Identifier: CA698022490
Gene: FOXO1 HGNC NCBI

Linked Data

dbSNP Id: rs1209747933
MyVariant Identifiers: chr13:g.41218592G>C (hg19) chr13:g.40644455G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644455G>C , CM000675.2:g.40644455G>C GRCh38
NC_000013.10:g.41218592G>C , CM000675.1:g.41218592G>C GRCh37
NC_000013.9:g.40116592G>C NCBI36
NG_023244.1:g.27143C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379561.6:c.630+21128C>G MANE Select ENSP00000368880.4:n.630+21128C>G
ENST00000655267.1:n.333+21128C>G
ENST00000660760.1:n.296-11207C>G
ENST00000379561.5:c.630+21128C>G ENSP00000368880.4:n.630+21128C>G
NM_002015.3:c.630+21128C>G NP_002006.2:n.630+21128C>G
XR_941536.1:n.1226+884C>G
NM_002015.4:c.630+21128C>G MANE Select NP_002006.2:n.630+21128C>G
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