Canonical Allele Identifier: CA323431393

Gene: FBXO7

Linked Data

• dbSNP Id: rs577331850
• gnomAD v3: 22-32484386-T-A
• gnomAD v4: 22-32484386-T-A
• MyVariant Identifiers: chr22:g.32880373T>A (hg19) ; chr22:g.32484386T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32484386T>A , CM000684.2:g.32484386T>A	GRCh38
NC_000022.10:g.32880373T>A , CM000684.1:g.32880373T>A	GRCh37
NC_000022.9:g.31210373T>A	NCBI36
NG_016001.1:g.14667T>A
NG_016001.2:g.14667T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.645+262T>A MANE Select	ENSP00000266087.7:n.645+262T>A
ENST00000266087.11:c.645+262T>A	ENSP00000266087.7:n.645+262T>A
ENST00000397426.5:c.303+262T>A	ENSP00000380571.1:n.303+262T>A
ENST00000420700.5:c.*224+262T>A	ENSP00000406155.1:n.*224+262T>A
ENST00000425028.5:c.*343+262T>A	ENSP00000395823.1:n.*343+262T>A
ENST00000452138.3:c.408+262T>A	ENSP00000388547.2:n.408+262T>A
ENST00000492535.1:n.481+262T>A
NM_001033024.1:c.408+262T>A	NP_001028196.1:n.408+262T>A
NM_001257990.1:c.303+262T>A	NP_001244919.1:n.303+262T>A
NM_012179.3:c.645+262T>A	NP_036311.3:n.645+262T>A
XM_011530106.1:c.177+262T>A	XP_011528408.1:n.177+262T>A
XM_024452207.1:c.303+262T>A	XP_024307975.1:n.303+262T>A
NM_012179.4:c.645+262T>A MANE Select	NP_036311.3:n.645+262T>A
NM_001033024.2:c.408+262T>A	NP_001028196.1:n.408+262T>A
NM_001257990.2:c.303+262T>A	NP_001244919.1:n.303+262T>A