Canonical Allele Identifier: CA1025189896

Gene: FBXO7

Linked Data

• dbSNP Id: rs2057485889
• gnomAD v3: 22-32484496-C-G
• gnomAD v4: 22-32484496-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32484496C>G , CM000684.2:g.32484496C>G	GRCh38
NC_000022.10:g.32880483C>G , CM000684.1:g.32880483C>G	GRCh37
NC_000022.9:g.31210483C>G	NCBI36
NG_016001.1:g.14777C>G
NG_016001.2:g.14777C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.645+372C>G MANE Select	ENSP00000266087.7:n.645+372C>G
ENST00000266087.11:c.645+372C>G	ENSP00000266087.7:n.645+372C>G
ENST00000397426.5:c.303+372C>G	ENSP00000380571.1:n.303+372C>G
ENST00000420700.5:c.*224+372C>G	ENSP00000406155.1:n.*224+372C>G
ENST00000425028.5:c.*343+372C>G	ENSP00000395823.1:n.*343+372C>G
ENST00000452138.3:c.408+372C>G	ENSP00000388547.2:n.408+372C>G
ENST00000492535.1:n.481+372C>G
NM_001033024.1:c.408+372C>G	NP_001028196.1:n.408+372C>G
NM_001257990.1:c.303+372C>G	NP_001244919.1:n.303+372C>G
NM_012179.3:c.645+372C>G	NP_036311.3:n.645+372C>G
XM_011530106.1:c.177+372C>G	XP_011528408.1:n.177+372C>G
XM_024452207.1:c.303+372C>G	XP_024307975.1:n.303+372C>G
NM_012179.4:c.645+372C>G MANE Select	NP_036311.3:n.645+372C>G
NM_001033024.2:c.408+372C>G	NP_001028196.1:n.408+372C>G
NM_001257990.2:c.303+372C>G	NP_001244919.1:n.303+372C>G