Canonical Allele Identifier: CA397763051

Gene: FBXO39

Linked Data

• MyVariant Identifiers: chr17:g.6684190A>T (hg19) ; chr17:g.6780871A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6780871A>T , CM000679.2:g.6780871A>T	GRCh38
NC_000017.10:g.6684190A>T , CM000679.1:g.6684190A>T	GRCh37
NC_000017.9:g.6624914A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321535.5:c.1003A>T MANE Select	ENSP00000321386.4:p.Thr335Ser
ENST00000321535.4:c.1003A>T	ENSP00000321386.4:p.Thr335Ser
NM_153230.2:c.1003A>T	NP_694962.1:p.Thr335Ser
XM_011523697.1:c.1003A>T	XP_011521999.1:p.Thr335Ser
XR_243544.3:n.1181A>T
NM_153230.3:c.1003A>T MANE Select	NP_694962.1:p.Thr335Ser