Canonical Allele Identifier: CA397762826
Gene: FBXO39 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780836G>C , CM000679.2:g.6780836G>C GRCh38
NC_000017.10:g.6684155G>C , CM000679.1:g.6684155G>C GRCh37
NC_000017.9:g.6624879G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.968G>C MANE Select ENSP00000321386.4:p.Cys323Ser
ENST00000321535.4:c.968G>C ENSP00000321386.4:p.Cys323Ser
NM_153230.2:c.968G>C NP_694962.1:p.Cys323Ser
XM_011523697.1:c.968G>C XP_011521999.1:p.Cys323Ser
XR_243544.3:n.1146G>C
NM_153230.3:c.968G>C MANE Select NP_694962.1:p.Cys323Ser