Canonical Allele Identifier: CA2401984988
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474725C= , CM000684.2:g.32474725C= GRCh38
NC_000022.10:g.32870712C= , CM000684.1:g.32870712C= GRCh37
NC_000022.9:g.31200712C= NCBI36
NG_016001.1:g.5006C=
NG_016001.2:g.5006C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.11:c.-278C= ENSP00000266087.7:n.-278C=
ENST00000420700.5:c.-278C= ENSP00000406155.1:n.-278C=
NM_012179.3:c.-278C= NP_036311.3:n.-278C=
XM_011530106.1:c.-451C= XP_011528408.1:n.-451C=
XM_024452207.1:c.-468C= XP_024307975.1:n.-468C=