Canonical Allele Identifier: CA2245513432
Gene: FBXO39 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780460C= , CM000679.2:g.6780460C= GRCh38
NC_000017.10:g.6683779C= , CM000679.1:g.6683779C= GRCh37
NC_000017.9:g.6624503C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.592C= MANE Select ENSP00000321386.4:p.Leu198=
ENST00000321535.4:c.592C= ENSP00000321386.4:p.Leu198=
NM_153230.2:c.592C= NP_694962.1:p.Leu198=
XM_011523697.1:c.592C= XP_011521999.1:p.Leu198=
XR_243544.3:n.770C=
NM_153230.3:c.592C= MANE Select NP_694962.1:p.Leu198=
Search 100 bp 5'
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