Canonical Allele Identifier: CA411329985
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs1203076750

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475097A>G , CM000684.2:g.32475097A>G GRCh38
NC_000022.10:g.32871084A>G , CM000684.1:g.32871084A>G GRCh37
NC_000022.9:g.31201084A>G NCBI36
NG_016001.1:g.5378A>G
NG_016001.2:g.5378A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.95A>G MANE Select ENSP00000266087.7:p.Gln32Arg
ENST00000266087.11:c.95A>G ENSP00000266087.7:p.Gln32Arg
ENST00000420700.5:c.95A>G ENSP00000406155.1:p.Gln32Arg
ENST00000425028.5:c.95A>G ENSP00000395823.1:p.Gln32Arg
ENST00000492535.1:n.83A>G
NM_012179.3:c.95A>G NP_036311.3:p.Gln32Arg
XM_011530106.1:c.-79A>G XP_011528408.1:n.-79A>G
XM_024452207.1:c.-96A>G XP_024307975.1:n.-96A>G
NM_012179.4:c.95A>G MANE Select NP_036311.3:p.Gln32Arg