Canonical Allele Identifier: CA397763214

Gene: FBXO39

Linked Data

• MyVariant Identifiers: chr17:g.6684212T>G (hg19) ; chr17:g.6780893T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6780893T>G , CM000679.2:g.6780893T>G	GRCh38
NC_000017.10:g.6684212T>G , CM000679.1:g.6684212T>G	GRCh37
NC_000017.9:g.6624936T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321535.5:c.1023+2T>G MANE Select	ENSP00000321386.4:n.1023+2T>G
ENST00000321535.4:c.1023+2T>G	ENSP00000321386.4:n.1023+2T>G
NM_153230.2:c.1023+2T>G	NP_694962.1:n.1023+2T>G
XM_011523697.1:c.1023+2T>G	XP_011521999.1:n.1023+2T>G
XR_243544.3:n.1201+2T>G
NM_153230.3:c.1023+2T>G MANE Select	NP_694962.1:n.1023+2T>G