Canonical Allele Identifier: CA411329931
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs2057417237

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475072G>A , CM000684.2:g.32475072G>A GRCh38
NC_000022.10:g.32871059G>A , CM000684.1:g.32871059G>A GRCh37
NC_000022.9:g.31201059G>A NCBI36
NG_016001.1:g.5353G>A
NG_016001.2:g.5353G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.70G>A MANE Select ENSP00000266087.7:p.Gly24Arg
ENST00000266087.11:c.70G>A ENSP00000266087.7:p.Gly24Arg
ENST00000420700.5:c.70G>A ENSP00000406155.1:p.Gly24Arg
ENST00000425028.5:c.70G>A ENSP00000395823.1:p.Gly24Arg
ENST00000492535.1:n.58G>A
NM_012179.3:c.70G>A NP_036311.3:p.Gly24Arg
XM_011530106.1:c.-104G>A XP_011528408.1:n.-104G>A
XM_024452207.1:c.-121G>A XP_024307975.1:n.-121G>A
NM_012179.4:c.70G>A MANE Select NP_036311.3:p.Gly24Arg