Canonical Allele Identifier: CA397761802
Gene: FBXO39 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780532A>C , CM000679.2:g.6780532A>C GRCh38
NC_000017.10:g.6683851A>C , CM000679.1:g.6683851A>C GRCh37
NC_000017.9:g.6624575A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.664A>C MANE Select ENSP00000321386.4:p.Thr222Pro
ENST00000321535.4:c.664A>C ENSP00000321386.4:p.Thr222Pro
NM_153230.2:c.664A>C NP_694962.1:p.Thr222Pro
XM_011523697.1:c.664A>C XP_011521999.1:p.Thr222Pro
XR_243544.3:n.842A>C
NM_153230.3:c.664A>C MANE Select NP_694962.1:p.Thr222Pro