Canonical Allele Identifier: CA2245513881
Gene: FBXO39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780776T= , CM000679.2:g.6780776T= GRCh38
NC_000017.10:g.6684095T= , CM000679.1:g.6684095T= GRCh37
NC_000017.9:g.6624819T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.908T= MANE Select ENSP00000321386.4:p.Leu303=
ENST00000321535.4:c.908T= ENSP00000321386.4:p.Leu303=
NM_153230.2:c.908T= NP_694962.1:p.Leu303=
XM_011523697.1:c.908T= XP_011521999.1:p.Leu303=
XR_243544.3:n.1086T=
NM_153230.3:c.908T= MANE Select NP_694962.1:p.Leu303=