Canonical Allele Identifier: CA497690047
Gene: FBXO39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6683715G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780396G>A , CM000679.2:g.6780396G>A GRCh38
NC_000017.10:g.6683715G>A , CM000679.1:g.6683715G>A GRCh37
NC_000017.9:g.6624439G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.528G>A MANE Select ENSP00000321386.4:p.Val176=
ENST00000321535.4:c.528G>A ENSP00000321386.4:p.Val176=
NM_153230.2:c.528G>A NP_694962.1:p.Val176=
XM_011523697.1:c.528G>A XP_011521999.1:p.Val176=
XR_243544.3:n.706G>A
NM_153230.3:c.528G>A MANE Select NP_694962.1:p.Val176=
Search 100 bp 5'
Search 100 bp 3'