Canonical Allele Identifier: CA2245513498
Gene: FBXO39 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780529T= , CM000679.2:g.6780529T= GRCh38
NC_000017.10:g.6683848T= , CM000679.1:g.6683848T= GRCh37
NC_000017.9:g.6624572T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.661T= MANE Select ENSP00000321386.4:p.Ser221=
ENST00000321535.4:c.661T= ENSP00000321386.4:p.Ser221=
NM_153230.2:c.661T= NP_694962.1:p.Ser221=
XM_011523697.1:c.661T= XP_011521999.1:p.Ser221=
XR_243544.3:n.839T=
NM_153230.3:c.661T= MANE Select NP_694962.1:p.Ser221=
Search 100 bp 5'
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