Canonical Allele Identifier: CA514294284

Gene: FBXO7

Linked Data

• dbSNP Id: rs2057416717
• gnomAD v4: 22-32475023-T-G
• MyVariant Identifiers: chr22:g.32871010T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32475023T>G , CM000684.2:g.32475023T>G	GRCh38
NC_000022.10:g.32871010T>G , CM000684.1:g.32871010T>G	GRCh37
NC_000022.9:g.31201010T>G	NCBI36
NG_016001.1:g.5304T>G
NG_016001.2:g.5304T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.21T>G MANE Select	ENSP00000266087.7:p.Leu7=
ENST00000266087.11:c.21T>G	ENSP00000266087.7:p.Leu7=
ENST00000420700.5:c.21T>G	ENSP00000406155.1:p.Leu7=
ENST00000425028.5:c.21T>G	ENSP00000395823.1:p.Leu7=
ENST00000492535.1:n.9T>G
NM_012179.3:c.21T>G	NP_036311.3:p.Leu7=
XM_011530106.1:c.-153T>G	XP_011528408.1:n.-153T>G
XM_024452207.1:c.-170T>G	XP_024307975.1:n.-170T>G
NM_012179.4:c.21T>G MANE Select	NP_036311.3:p.Leu7=