Canonical Allele Identifier: CA397762374
Gene: FBXO39 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780687G>T , CM000679.2:g.6780687G>T GRCh38
NC_000017.10:g.6684006G>T , CM000679.1:g.6684006G>T GRCh37
NC_000017.9:g.6624730G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.819G>T MANE Select ENSP00000321386.4:p.Trp273Cys
ENST00000321535.4:c.819G>T ENSP00000321386.4:p.Trp273Cys
NM_153230.2:c.819G>T NP_694962.1:p.Trp273Cys
XM_011523697.1:c.819G>T XP_011521999.1:p.Trp273Cys
XR_243544.3:n.997G>T
NM_153230.3:c.819G>T MANE Select NP_694962.1:p.Trp273Cys