Canonical Allele Identifier: CA10201292

Gene: FBXO7

Linked Data

• dbSNP Id: rs747840429
• ExAC: 22:32871007 G / A
• gnomAD v2: 22-32871007-G-A
• gnomAD v4: 22-32475020-G-A
• MyVariant Identifiers: chr22:g.32871007G>A (hg19) ; chr22:g.32475020G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32475020G>A , CM000684.2:g.32475020G>A	GRCh38
NC_000022.10:g.32871007G>A , CM000684.1:g.32871007G>A	GRCh37
NC_000022.9:g.31201007G>A	NCBI36
NG_016001.1:g.5301G>A
NG_016001.2:g.5301G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.18G>A MANE Select	ENSP00000266087.7:p.Arg6=
ENST00000266087.11:c.18G>A	ENSP00000266087.7:p.Arg6=
ENST00000420700.5:c.18G>A	ENSP00000406155.1:p.Arg6=
ENST00000425028.5:c.18G>A	ENSP00000395823.1:p.Arg6=
ENST00000492535.1:n.6G>A
NM_012179.3:c.18G>A	NP_036311.3:p.Arg6=
XM_011530106.1:c.-156G>A	XP_011528408.1:n.-156G>A
XM_024452207.1:c.-173G>A	XP_024307975.1:n.-173G>A
NM_012179.4:c.18G>A MANE Select	NP_036311.3:p.Arg6=