Canonical Allele Identifier: CA253301
Gene: FBXO7 HGNC NCBI

Linked Data

ClinVar Variation Id: 4811
ClinVar RCV Id: RCV000005080
dbSNP Id: rs121918305

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475067C>T , CM000684.2:g.32475067C>T GRCh38
NC_000022.10:g.32871054C>T , CM000684.1:g.32871054C>T GRCh37
NC_000022.9:g.31201054C>T NCBI36
NG_016001.1:g.5348C>T
NG_016001.2:g.5348C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.65C>T MANE Select ENSP00000266087.7:p.Thr22Met
ENST00000266087.11:c.65C>T ENSP00000266087.7:p.Thr22Met
ENST00000420700.5:c.65C>T ENSP00000406155.1:p.Thr22Met
ENST00000425028.5:c.65C>T ENSP00000395823.1:p.Thr22Met
ENST00000492535.1:n.53C>T
NM_012179.3:c.65C>T NP_036311.3:p.Thr22Met
XM_011530106.1:c.-109C>T XP_011528408.1:n.-109C>T
XM_024452207.1:c.-126C>T XP_024307975.1:n.-126C>T
NM_012179.4:c.65C>T MANE Select NP_036311.3:p.Thr22Met