Canonical Allele Identifier: CA2245513822
Gene: FBXO39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780730T= , CM000679.2:g.6780730T= GRCh38
NC_000017.10:g.6684049T= , CM000679.1:g.6684049T= GRCh37
NC_000017.9:g.6624773T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.862T= MANE Select ENSP00000321386.4:p.Phe288=
ENST00000321535.4:c.862T= ENSP00000321386.4:p.Phe288=
NM_153230.2:c.862T= NP_694962.1:p.Phe288=
XM_011523697.1:c.862T= XP_011521999.1:p.Phe288=
XR_243544.3:n.1040T=
NM_153230.3:c.862T= MANE Select NP_694962.1:p.Phe288=