Canonical Allele Identifier: CA411329893
Gene: FBXO7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2585291
ClinVar RCV Id: RCV003337907
dbSNP Id: rs1412416225

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475054G>A , CM000684.2:g.32475054G>A GRCh38
NC_000022.10:g.32871041G>A , CM000684.1:g.32871041G>A GRCh37
NC_000022.9:g.31201041G>A NCBI36
NG_016001.1:g.5335G>A
NG_016001.2:g.5335G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.52G>A MANE Select ENSP00000266087.7:p.Glu18Lys
ENST00000266087.11:c.52G>A ENSP00000266087.7:p.Glu18Lys
ENST00000420700.5:c.52G>A ENSP00000406155.1:p.Glu18Lys
ENST00000425028.5:c.52G>A ENSP00000395823.1:p.Glu18Lys
ENST00000492535.1:n.40G>A
NM_012179.3:c.52G>A NP_036311.3:p.Glu18Lys
XM_011530106.1:c.-122G>A XP_011528408.1:n.-122G>A
XM_024452207.1:c.-139G>A XP_024307975.1:n.-139G>A
NM_012179.4:c.52G>A MANE Select NP_036311.3:p.Glu18Lys