Canonical Allele Identifier: CA323431384

Gene: FBXO7

Linked Data

• dbSNP Id: rs556798436
• gnomAD v3: 22-32484360-G-A
• gnomAD v4: 22-32484360-G-A
• MyVariant Identifiers: chr22:g.32880347G>A (hg19) ; chr22:g.32484360G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32484360G>A , CM000684.2:g.32484360G>A	GRCh38
NC_000022.10:g.32880347G>A , CM000684.1:g.32880347G>A	GRCh37
NC_000022.9:g.31210347G>A	NCBI36
NG_016001.1:g.14641G>A
NG_016001.2:g.14641G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.645+236G>A MANE Select	ENSP00000266087.7:n.645+236G>A
ENST00000266087.11:c.645+236G>A	ENSP00000266087.7:n.645+236G>A
ENST00000397426.5:c.303+236G>A	ENSP00000380571.1:n.303+236G>A
ENST00000420700.5:c.*224+236G>A	ENSP00000406155.1:n.*224+236G>A
ENST00000425028.5:c.*343+236G>A	ENSP00000395823.1:n.*343+236G>A
ENST00000452138.3:c.408+236G>A	ENSP00000388547.2:n.408+236G>A
ENST00000492535.1:n.481+236G>A
NM_001033024.1:c.408+236G>A	NP_001028196.1:n.408+236G>A
NM_001257990.1:c.303+236G>A	NP_001244919.1:n.303+236G>A
NM_012179.3:c.645+236G>A	NP_036311.3:n.645+236G>A
XM_011530106.1:c.177+236G>A	XP_011528408.1:n.177+236G>A
XM_024452207.1:c.303+236G>A	XP_024307975.1:n.303+236G>A
NM_012179.4:c.645+236G>A MANE Select	NP_036311.3:n.645+236G>A
NM_001033024.2:c.408+236G>A	NP_001028196.1:n.408+236G>A
NM_001257990.2:c.303+236G>A	NP_001244919.1:n.303+236G>A