Canonical Allele Identifier: CA2245513766
Gene: FBXO39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780697G= , CM000679.2:g.6780697G= GRCh38
NC_000017.10:g.6684016G= , CM000679.1:g.6684016G= GRCh37
NC_000017.9:g.6624740G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.829G= MANE Select ENSP00000321386.4:p.Ala277=
ENST00000321535.4:c.829G= ENSP00000321386.4:p.Ala277=
NM_153230.2:c.829G= NP_694962.1:p.Ala277=
XM_011523697.1:c.829G= XP_011521999.1:p.Ala277=
XR_243544.3:n.1007G=
NM_153230.3:c.829G= MANE Select NP_694962.1:p.Ala277=