Canonical Allele Identifier: CA397762935
Gene: FBXO39 HGNC NCBI

Linked Data

dbSNP Id: rs200108762
gnomAD v2: 17-6684170-C-G
gnomAD v4: 17-6780851-C-G
MyVariant Identifiers: chr17:g.6684170C>G (hg19) chr17:g.6780851C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780851C>G , CM000679.2:g.6780851C>G GRCh38
NC_000017.10:g.6684170C>G , CM000679.1:g.6684170C>G GRCh37
NC_000017.9:g.6624894C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.983C>G MANE Select ENSP00000321386.4:p.Thr328Ser
ENST00000321535.4:c.983C>G ENSP00000321386.4:p.Thr328Ser
NM_153230.2:c.983C>G NP_694962.1:p.Thr328Ser
XM_011523697.1:c.983C>G XP_011521999.1:p.Thr328Ser
XR_243544.3:n.1161C>G
NM_153230.3:c.983C>G MANE Select NP_694962.1:p.Thr328Ser
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