Canonical Allele Identifier: CA397762331
Gene: FBXO39 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780670A>C , CM000679.2:g.6780670A>C GRCh38
NC_000017.10:g.6683989A>C , CM000679.1:g.6683989A>C GRCh37
NC_000017.9:g.6624713A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.802A>C MANE Select ENSP00000321386.4:p.Ile268Leu
ENST00000321535.4:c.802A>C ENSP00000321386.4:p.Ile268Leu
NM_153230.2:c.802A>C NP_694962.1:p.Ile268Leu
XM_011523697.1:c.802A>C XP_011521999.1:p.Ile268Leu
XR_243544.3:n.980A>C
NM_153230.3:c.802A>C MANE Select NP_694962.1:p.Ile268Leu