Canonical Allele Identifier: CA397762579

Gene: FBXO39

Linked Data

• MyVariant Identifiers: chr17:g.6684103A>G (hg19) ; chr17:g.6780784A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6780784A>G , CM000679.2:g.6780784A>G	GRCh38
NC_000017.10:g.6684103A>G , CM000679.1:g.6684103A>G	GRCh37
NC_000017.9:g.6624827A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321535.5:c.916A>G MANE Select	ENSP00000321386.4:p.Ile306Val
ENST00000321535.4:c.916A>G	ENSP00000321386.4:p.Ile306Val
NM_153230.2:c.916A>G	NP_694962.1:p.Ile306Val
XM_011523697.1:c.916A>G	XP_011521999.1:p.Ile306Val
XR_243544.3:n.1094A>G
NM_153230.3:c.916A>G MANE Select	NP_694962.1:p.Ile306Val