Canonical Allele Identifier: CA397762601
Gene: FBXO39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6684114G>C (hg19) chr17:g.6780795G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780795G>C , CM000679.2:g.6780795G>C GRCh38
NC_000017.10:g.6684114G>C , CM000679.1:g.6684114G>C GRCh37
NC_000017.9:g.6624838G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.927G>C MANE Select ENSP00000321386.4:p.Arg309Ser
ENST00000321535.4:c.927G>C ENSP00000321386.4:p.Arg309Ser
NM_153230.2:c.927G>C NP_694962.1:p.Arg309Ser
XM_011523697.1:c.927G>C XP_011521999.1:p.Arg309Ser
XR_243544.3:n.1105G>C
NM_153230.3:c.927G>C MANE Select NP_694962.1:p.Arg309Ser
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Search 100 bp 3'