Canonical Allele Identifier: CA2245513718
Gene: FBXO39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780669C= , CM000679.2:g.6780669C= GRCh38
NC_000017.10:g.6683988C= , CM000679.1:g.6683988C= GRCh37
NC_000017.9:g.6624712C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.801C= MANE Select ENSP00000321386.4:p.Val267=
ENST00000321535.4:c.801C= ENSP00000321386.4:p.Val267=
NM_153230.2:c.801C= NP_694962.1:p.Val267=
XM_011523697.1:c.801C= XP_011521999.1:p.Val267=
XR_243544.3:n.979C=
NM_153230.3:c.801C= MANE Select NP_694962.1:p.Val267=