Canonical Allele Identifier: CA624682715
Gene: FBXO39 HGNC NCBI

Linked Data

dbSNP Id: rs1244091380
gnomAD v2: 17-6684237-G-A
gnomAD v4: 17-6780918-G-A
MyVariant Identifiers: chr17:g.6684237G>A (hg19) chr17:g.6780918G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780918G>A , CM000679.2:g.6780918G>A GRCh38
NC_000017.10:g.6684237G>A , CM000679.1:g.6684237G>A GRCh37
NC_000017.9:g.6624961G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.1023+27G>A MANE Select ENSP00000321386.4:n.1023+27G>A
ENST00000321535.4:c.1023+27G>A ENSP00000321386.4:n.1023+27G>A
NM_153230.2:c.1023+27G>A NP_694962.1:n.1023+27G>A
XM_011523697.1:c.1023+27G>A XP_011521999.1:n.1023+27G>A
XR_243544.3:n.1201+27G>A
NM_153230.3:c.1023+27G>A MANE Select NP_694962.1:n.1023+27G>A
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