Canonical Allele Identifier: CA639098949
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs1568969837

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475118_32475146del , CM000684.2:g.32475118_32475146del GRCh38
NC_000022.10:g.32871105_32871133del , CM000684.1:g.32871105_32871133del GRCh37
NC_000022.9:g.31201105_31201133del NCBI36
NG_016001.1:g.5399_5427del
NG_016001.2:g.5399_5427del

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.116_122+22del
ENST00000266087.11:c.116_122+22del
ENST00000420700.5:c.116_122+22del
ENST00000425028.5:c.116_122+22del
ENST00000492535.1:n.104_110+22del
NM_012179.3:c.116_122+22del
XM_011530106.1:c.-58_-52+22del
XM_024452207.1:c.-75_-69+22del
NM_012179.4:c.116_122+22del