Canonical Allele Identifier: CA2656311369
Gene: FBXO7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474893G>A , CM000684.2:g.32474893G>A GRCh38
NC_000022.10:g.32870880G>A , CM000684.1:g.32870880G>A GRCh37
NC_000022.9:g.31200880G>A NCBI36
NG_016001.1:g.5174G>A
NG_016001.2:g.5174G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.-110G>A MANE Select ENSP00000266087.7:n.-110G>A
ENST00000266087.11:c.-110G>A ENSP00000266087.7:n.-110G>A
ENST00000420700.5:c.-110G>A ENSP00000406155.1:n.-110G>A
ENST00000425028.5:c.-110G>A ENSP00000395823.1:n.-110G>A
NM_012179.3:c.-110G>A NP_036311.3:n.-110G>A
XM_011530106.1:c.-283G>A XP_011528408.1:n.-283G>A
XM_024452207.1:c.-300G>A XP_024307975.1:n.-300G>A
NM_012179.4:c.-110G>A MANE Select NP_036311.3:n.-110G>A