Canonical Allele Identifier: CA497596058
Gene: FBXO39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6684168C>G (hg19)
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Genomic Alleles

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

Transcript Alleles

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