Canonical Allele Identifier: CA752552596

Gene: FBXO7

Linked Data

• dbSNP Id: rs1418193951
• gnomAD v3: 22-32484528-C-G
• gnomAD v4: 22-32484528-C-G
• MyVariant Identifiers: chr22:g.32880515C>G (hg19) ; chr22:g.32484528C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32484528C>G , CM000684.2:g.32484528C>G	GRCh38
NC_000022.10:g.32880515C>G , CM000684.1:g.32880515C>G	GRCh37
NC_000022.9:g.31210515C>G	NCBI36
NG_016001.1:g.14809C>G
NG_016001.2:g.14809C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.645+404C>G MANE Select	ENSP00000266087.7:n.645+404C>G
ENST00000266087.11:c.645+404C>G	ENSP00000266087.7:n.645+404C>G
ENST00000397426.5:c.303+404C>G	ENSP00000380571.1:n.303+404C>G
ENST00000420700.5:c.*224+404C>G	ENSP00000406155.1:n.*224+404C>G
ENST00000425028.5:c.*343+404C>G	ENSP00000395823.1:n.*343+404C>G
ENST00000452138.3:c.408+404C>G	ENSP00000388547.2:n.408+404C>G
ENST00000492535.1:n.481+404C>G
NM_001033024.1:c.408+404C>G	NP_001028196.1:n.408+404C>G
NM_001257990.1:c.303+404C>G	NP_001244919.1:n.303+404C>G
NM_012179.3:c.645+404C>G	NP_036311.3:n.645+404C>G
XM_011530106.1:c.177+404C>G	XP_011528408.1:n.177+404C>G
XM_024452207.1:c.303+404C>G	XP_024307975.1:n.303+404C>G
NM_012179.4:c.645+404C>G MANE Select	NP_036311.3:n.645+404C>G
NM_001033024.2:c.408+404C>G	NP_001028196.1:n.408+404C>G
NM_001257990.2:c.303+404C>G	NP_001244919.1:n.303+404C>G