Canonical Allele Identifier: CA397762941
Gene: FBXO39 HGNC NCBI

Linked Data

dbSNP Id: rs1976501004
MyVariant Identifiers: chr17:g.6684172C>G (hg19) chr17:g.6780853C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780853C>G , CM000679.2:g.6780853C>G GRCh38
NC_000017.10:g.6684172C>G , CM000679.1:g.6684172C>G GRCh37
NC_000017.9:g.6624896C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.985C>G MANE Select ENSP00000321386.4:p.Leu329Val
ENST00000321535.4:c.985C>G ENSP00000321386.4:p.Leu329Val
NM_153230.2:c.985C>G NP_694962.1:p.Leu329Val
XM_011523697.1:c.985C>G XP_011521999.1:p.Leu329Val
XR_243544.3:n.1163C>G
NM_153230.3:c.985C>G MANE Select NP_694962.1:p.Leu329Val
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