Canonical Allele Identifier: CA397761492
Gene: FBXO39 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780478T>G , CM000679.2:g.6780478T>G GRCh38
NC_000017.10:g.6683797T>G , CM000679.1:g.6683797T>G GRCh37
NC_000017.9:g.6624521T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.610T>G MANE Select ENSP00000321386.4:p.Phe204Val
ENST00000321535.4:c.610T>G ENSP00000321386.4:p.Phe204Val
NM_153230.2:c.610T>G NP_694962.1:p.Phe204Val
XM_011523697.1:c.610T>G XP_011521999.1:p.Phe204Val
XR_243544.3:n.788T>G
NM_153230.3:c.610T>G MANE Select NP_694962.1:p.Phe204Val