Canonical Allele Identifier: CA2245513980
Gene: FBXO39 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780846A= , CM000679.2:g.6780846A= GRCh38
NC_000017.10:g.6684165A= , CM000679.1:g.6684165A= GRCh37
NC_000017.9:g.6624889A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.978A= MANE Select ENSP00000321386.4:p.Arg326=
ENST00000321535.4:c.978A= ENSP00000321386.4:p.Arg326=
NM_153230.2:c.978A= NP_694962.1:p.Arg326=
XM_011523697.1:c.978A= XP_011521999.1:p.Arg326=
XR_243544.3:n.1156A=
NM_153230.3:c.978A= MANE Select NP_694962.1:p.Arg326=
Search 100 bp 5'
Search 100 bp 3'