Canonical Allele Identifier: CA2245513535
Gene: FBXO39 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780559C= , CM000679.2:g.6780559C= GRCh38
NC_000017.10:g.6683878C= , CM000679.1:g.6683878C= GRCh37
NC_000017.9:g.6624602C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.691C= MANE Select ENSP00000321386.4:p.Leu231=
ENST00000321535.4:c.691C= ENSP00000321386.4:p.Leu231=
NM_153230.2:c.691C= NP_694962.1:p.Leu231=
XM_011523697.1:c.691C= XP_011521999.1:p.Leu231=
XR_243544.3:n.869C=
NM_153230.3:c.691C= MANE Select NP_694962.1:p.Leu231=
Search 100 bp 5'
Search 100 bp 3'