Canonical Allele Identifier: CA411329938
Gene: FBXO7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475075C>G , CM000684.2:g.32475075C>G GRCh38
NC_000022.10:g.32871062C>G , CM000684.1:g.32871062C>G GRCh37
NC_000022.9:g.31201062C>G NCBI36
NG_016001.1:g.5356C>G
NG_016001.2:g.5356C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.73C>G MANE Select ENSP00000266087.7:p.His25Asp
ENST00000266087.11:c.73C>G ENSP00000266087.7:p.His25Asp
ENST00000420700.5:c.73C>G ENSP00000406155.1:p.His25Asp
ENST00000425028.5:c.73C>G ENSP00000395823.1:p.His25Asp
ENST00000492535.1:n.61C>G
NM_012179.3:c.73C>G NP_036311.3:p.His25Asp
XM_011530106.1:c.-101C>G XP_011528408.1:n.-101C>G
XM_024452207.1:c.-118C>G XP_024307975.1:n.-118C>G
NM_012179.4:c.73C>G MANE Select NP_036311.3:p.His25Asp