Canonical Allele Identifier: CA497690123

Gene: FBXO39

Linked Data

• MyVariant Identifiers: chr17:g.6683817C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6780498C>T , CM000679.2:g.6780498C>T	GRCh38
NC_000017.10:g.6683817C>T , CM000679.1:g.6683817C>T	GRCh37
NC_000017.9:g.6624541C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321535.5:c.630C>T MANE Select	ENSP00000321386.4:p.Val210=
ENST00000321535.4:c.630C>T	ENSP00000321386.4:p.Val210=
NM_153230.2:c.630C>T	NP_694962.1:p.Val210=
XM_011523697.1:c.630C>T	XP_011521999.1:p.Val210=
XR_243544.3:n.808C>T
NM_153230.3:c.630C>T MANE Select	NP_694962.1:p.Val210=