Canonical Allele Identifier: CA397762783
Gene: FBXO39 HGNC NCBI

Linked Data

gnomAD v4: 17-6780827-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780827A>G , CM000679.2:g.6780827A>G GRCh38
NC_000017.10:g.6684146A>G , CM000679.1:g.6684146A>G GRCh37
NC_000017.9:g.6624870A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.959A>G MANE Select ENSP00000321386.4:p.Asp320Gly
ENST00000321535.4:c.959A>G ENSP00000321386.4:p.Asp320Gly
NM_153230.2:c.959A>G NP_694962.1:p.Asp320Gly
XM_011523697.1:c.959A>G XP_011521999.1:p.Asp320Gly
XR_243544.3:n.1137A>G
NM_153230.3:c.959A>G MANE Select NP_694962.1:p.Asp320Gly