Canonical Allele Identifier: CA397762708

Gene: FBXO39

Linked Data

• MyVariant Identifiers: chr17:g.6684134G>T (hg19) ; chr17:g.6780815G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6780815G>T , CM000679.2:g.6780815G>T	GRCh38
NC_000017.10:g.6684134G>T , CM000679.1:g.6684134G>T	GRCh37
NC_000017.9:g.6624858G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321535.5:c.947G>T MANE Select	ENSP00000321386.4:p.Cys316Phe
ENST00000321535.4:c.947G>T	ENSP00000321386.4:p.Cys316Phe
NM_153230.2:c.947G>T	NP_694962.1:p.Cys316Phe
XM_011523697.1:c.947G>T	XP_011521999.1:p.Cys316Phe
XR_243544.3:n.1125G>T
NM_153230.3:c.947G>T MANE Select	NP_694962.1:p.Cys316Phe