Canonical Allele Identifier: CA497596057
Gene: FBXO39 HGNC NCBI

Linked Data

COSMIC: COSM302211
MyVariant Identifiers: chr17:g.6684168C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780849C>A , CM000679.2:g.6780849C>A GRCh38
NC_000017.10:g.6684168C>A , CM000679.1:g.6684168C>A GRCh37
NC_000017.9:g.6624892C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.981C>A MANE Select ENSP00000321386.4:p.Pro327=
ENST00000321535.4:c.981C>A ENSP00000321386.4:p.Pro327=
NM_153230.2:c.981C>A NP_694962.1:p.Pro327=
XM_011523697.1:c.981C>A XP_011521999.1:p.Pro327=
XR_243544.3:n.1159C>A
NM_153230.3:c.981C>A MANE Select NP_694962.1:p.Pro327=
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