Canonical Allele Identifier: CA2401985166
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474973T= , CM000684.2:g.32474973T= GRCh38
NC_000022.10:g.32870960T= , CM000684.1:g.32870960T= GRCh37
NC_000022.9:g.31200960T= NCBI36
NG_016001.1:g.5254T=
NG_016001.2:g.5254T=

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.-30T= MANE Select ENSP00000266087.7:n.-30T=
ENST00000266087.11:c.-30T= ENSP00000266087.7:n.-30T=
ENST00000420700.5:c.-30T= ENSP00000406155.1:n.-30T=
ENST00000425028.5:c.-30T= ENSP00000395823.1:n.-30T=
NM_012179.3:c.-30T= NP_036311.3:n.-30T=
XM_011530106.1:c.-203T= XP_011528408.1:n.-203T=
XM_024452207.1:c.-220T= XP_024307975.1:n.-220T=
NM_012179.4:c.-30T= MANE Select NP_036311.3:n.-30T=