Canonical Allele Identifier: CA2245513465
Gene: FBXO39 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780482G= , CM000679.2:g.6780482G= GRCh38
NC_000017.10:g.6683801G= , CM000679.1:g.6683801G= GRCh37
NC_000017.9:g.6624525G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.614G= MANE Select ENSP00000321386.4:p.Ser205=
ENST00000321535.4:c.614G= ENSP00000321386.4:p.Ser205=
NM_153230.2:c.614G= NP_694962.1:p.Ser205=
XM_011523697.1:c.614G= XP_011521999.1:p.Ser205=
XR_243544.3:n.792G=
NM_153230.3:c.614G= MANE Select NP_694962.1:p.Ser205=
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