Canonical Allele Identifier: CA397762460
Gene: FBXO39 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780728T>C , CM000679.2:g.6780728T>C GRCh38
NC_000017.10:g.6684047T>C , CM000679.1:g.6684047T>C GRCh37
NC_000017.9:g.6624771T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.860T>C MANE Select ENSP00000321386.4:p.Phe287Ser
ENST00000321535.4:c.860T>C ENSP00000321386.4:p.Phe287Ser
NM_153230.2:c.860T>C NP_694962.1:p.Phe287Ser
XM_011523697.1:c.860T>C XP_011521999.1:p.Phe287Ser
XR_243544.3:n.1038T>C
NM_153230.3:c.860T>C MANE Select NP_694962.1:p.Phe287Ser