Canonical Allele Identifier: CA2245513705
Gene: FBXO39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780661G= , CM000679.2:g.6780661G= GRCh38
NC_000017.10:g.6683980G= , CM000679.1:g.6683980G= GRCh37
NC_000017.9:g.6624704G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.793G= MANE Select ENSP00000321386.4:p.Gly265=
ENST00000321535.4:c.793G= ENSP00000321386.4:p.Gly265=
NM_153230.2:c.793G= NP_694962.1:p.Gly265=
XM_011523697.1:c.793G= XP_011521999.1:p.Gly265=
XR_243544.3:n.971G=
NM_153230.3:c.793G= MANE Select NP_694962.1:p.Gly265=