Canonical Allele Identifier: CA2245513942
Gene: FBXO39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780811A= , CM000679.2:g.6780811A= GRCh38
NC_000017.10:g.6684130A= , CM000679.1:g.6684130A= GRCh37
NC_000017.9:g.6624854A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.943A= MANE Select ENSP00000321386.4:p.Ser315=
ENST00000321535.4:c.943A= ENSP00000321386.4:p.Ser315=
NM_153230.2:c.943A= NP_694962.1:p.Ser315=
XM_011523697.1:c.943A= XP_011521999.1:p.Ser315=
XR_243544.3:n.1121A=
NM_153230.3:c.943A= MANE Select NP_694962.1:p.Ser315=