Canonical Allele Identifier: CA2401984991
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474729G= , CM000684.2:g.32474729G= GRCh38
NC_000022.10:g.32870716G= , CM000684.1:g.32870716G= GRCh37
NC_000022.9:g.31200716G= NCBI36
NG_016001.1:g.5010G=
NG_016001.2:g.5010G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.11:c.-274G= ENSP00000266087.7:n.-274G=
ENST00000420700.5:c.-274G= ENSP00000406155.1:n.-274G=
NM_012179.3:c.-274G= NP_036311.3:n.-274G=
XM_011530106.1:c.-447G= XP_011528408.1:n.-447G=
XM_024452207.1:c.-464G= XP_024307975.1:n.-464G=