Canonical Allele Identifier: CA2401985227
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475076A= , CM000684.2:g.32475076A= GRCh38
NC_000022.10:g.32871063A= , CM000684.1:g.32871063A= GRCh37
NC_000022.9:g.31201063A= NCBI36
NG_016001.1:g.5357A=
NG_016001.2:g.5357A=

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.74A= MANE Select ENSP00000266087.7:p.His25=
ENST00000266087.11:c.74A= ENSP00000266087.7:p.His25=
ENST00000420700.5:c.74A= ENSP00000406155.1:p.His25=
ENST00000425028.5:c.74A= ENSP00000395823.1:p.His25=
ENST00000492535.1:n.62A=
NM_012179.3:c.74A= NP_036311.3:p.His25=
XM_011530106.1:c.-100A= XP_011528408.1:n.-100A=
XM_024452207.1:c.-117A= XP_024307975.1:n.-117A=
NM_012179.4:c.74A= MANE Select NP_036311.3:p.His25=