Canonical Allele Identifier: CA411329934

Gene: FBXO7

Linked Data

• dbSNP Id: rs1411104257
• gnomAD v2: 22-32871060-G-A
• gnomAD v4: 22-32475073-G-A
• MyVariant Identifiers: chr22:g.32871060G>A (hg19) ; chr22:g.32475073G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32475073G>A , CM000684.2:g.32475073G>A	GRCh38
NC_000022.10:g.32871060G>A , CM000684.1:g.32871060G>A	GRCh37
NC_000022.9:g.31201060G>A	NCBI36
NG_016001.1:g.5354G>A
NG_016001.2:g.5354G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.71G>A MANE Select	ENSP00000266087.7:p.Gly24Glu
ENST00000266087.11:c.71G>A	ENSP00000266087.7:p.Gly24Glu
ENST00000420700.5:c.71G>A	ENSP00000406155.1:p.Gly24Glu
ENST00000425028.5:c.71G>A	ENSP00000395823.1:p.Gly24Glu
ENST00000492535.1:n.59G>A
NM_012179.3:c.71G>A	NP_036311.3:p.Gly24Glu
XM_011530106.1:c.-103G>A	XP_011528408.1:n.-103G>A
XM_024452207.1:c.-120G>A	XP_024307975.1:n.-120G>A
NM_012179.4:c.71G>A MANE Select	NP_036311.3:p.Gly24Glu