Canonical Allele Identifier: CA2401985346

Gene: FBXO7

Linked Data

• dbSNP Id: rs1601499924

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32475251A>G , CM000684.2:g.32475251A>G	GRCh38
NC_000022.10:g.32871238A>G , CM000684.1:g.32871238A>G	GRCh37
NC_000022.9:g.31201238A>G	NCBI36
NG_016001.1:g.5532A>G
NG_016001.2:g.5532A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.122+127A>G MANE Select	ENSP00000266087.7:n.122+127A>G
ENST00000266087.11:c.122+127A>G	ENSP00000266087.7:n.122+127A>G
ENST00000420700.5:c.122+127A>G	ENSP00000406155.1:n.122+127A>G
ENST00000425028.5:c.122+127A>G	ENSP00000395823.1:n.122+127A>G
ENST00000452138.3:c.-111A>G	ENSP00000388547.2:n.-111A>G
ENST00000492535.1:n.110+127A>G
NM_001033024.1:c.-111A>G	NP_001028196.1:n.-111A>G
NM_001257990.1:c.-368A>G	NP_001244919.1:n.-368A>G
NM_012179.3:c.122+127A>G	NP_036311.3:n.122+127A>G
XM_011530106.1:c.-52+127A>G	XP_011528408.1:n.-52+127A>G
XM_024452207.1:c.-69+127A>G	XP_024307975.1:n.-69+127A>G
NM_012179.4:c.122+127A>G MANE Select	NP_036311.3:n.122+127A>G