Canonical Allele Identifier: CA397762887
Gene: FBXO39 HGNC NCBI

Linked Data

dbSNP Id: rs1240897962
gnomAD v2: 17-6684164-G-A
gnomAD v4: 17-6780845-G-A
MyVariant Identifiers: chr17:g.6684164G>A (hg19) chr17:g.6780845G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780845G>A , CM000679.2:g.6780845G>A GRCh38
NC_000017.10:g.6684164G>A , CM000679.1:g.6684164G>A GRCh37
NC_000017.9:g.6624888G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.977G>A MANE Select ENSP00000321386.4:p.Arg326Lys
ENST00000321535.4:c.977G>A ENSP00000321386.4:p.Arg326Lys
NM_153230.2:c.977G>A NP_694962.1:p.Arg326Lys
XM_011523697.1:c.977G>A XP_011521999.1:p.Arg326Lys
XR_243544.3:n.1155G>A
NM_153230.3:c.977G>A MANE Select NP_694962.1:p.Arg326Lys
Search 100 bp 5'
Search 100 bp 3'