Canonical Allele Identifier: CA698022595
Gene: FOXO1 HGNC NCBI

Linked Data

dbSNP Id: rs1397645652
MyVariant Identifiers: chr13:g.41218718G>A (hg19) chr13:g.40644581G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644581G>A , CM000675.2:g.40644581G>A GRCh38
NC_000013.10:g.41218718G>A , CM000675.1:g.41218718G>A GRCh37
NC_000013.9:g.40116718G>A NCBI36
NG_023244.1:g.27017C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379561.6:c.630+21002C>T MANE Select ENSP00000368880.4:n.630+21002C>T
ENST00000655267.1:n.333+21002C>T
ENST00000660760.1:n.296-11333C>T
ENST00000379561.5:c.630+21002C>T ENSP00000368880.4:n.630+21002C>T
NM_002015.3:c.630+21002C>T NP_002006.2:n.630+21002C>T
XR_941536.1:n.1226+758C>T
NM_002015.4:c.630+21002C>T MANE Select NP_002006.2:n.630+21002C>T
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