Canonical Allele Identifier: CA2245513743
Gene: FBXO39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780682T= , CM000679.2:g.6780682T= GRCh38
NC_000017.10:g.6684001T= , CM000679.1:g.6684001T= GRCh37
NC_000017.9:g.6624725T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.814T= MANE Select ENSP00000321386.4:p.Ser272=
ENST00000321535.4:c.814T= ENSP00000321386.4:p.Ser272=
NM_153230.2:c.814T= NP_694962.1:p.Ser272=
XM_011523697.1:c.814T= XP_011521999.1:p.Ser272=
XR_243544.3:n.992T=
NM_153230.3:c.814T= MANE Select NP_694962.1:p.Ser272=