Canonical Allele Identifier: CA397762897
Gene: FBXO39 HGNC NCBI

Linked Data

dbSNP Id: rs1487160808
gnomAD v2: 17-6684165-A-T
gnomAD v4: 17-6780846-A-T
MyVariant Identifiers: chr17:g.6684165A>T (hg19) chr17:g.6780846A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780846A>T , CM000679.2:g.6780846A>T GRCh38
NC_000017.10:g.6684165A>T , CM000679.1:g.6684165A>T GRCh37
NC_000017.9:g.6624889A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.978A>T MANE Select ENSP00000321386.4:p.Arg326Ser
ENST00000321535.4:c.978A>T ENSP00000321386.4:p.Arg326Ser
NM_153230.2:c.978A>T NP_694962.1:p.Arg326Ser
XM_011523697.1:c.978A>T XP_011521999.1:p.Arg326Ser
XR_243544.3:n.1156A>T
NM_153230.3:c.978A>T MANE Select NP_694962.1:p.Arg326Ser
Search 100 bp 5'
Search 100 bp 3'