Canonical Allele Identifier: CA2245514091

Gene: FBXO39

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6780919C= , CM000679.2:g.6780919C=	GRCh38
NC_000017.10:g.6684238C= , CM000679.1:g.6684238C=	GRCh37
NC_000017.9:g.6624962C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321535.5:c.1023+28C= MANE Select	ENSP00000321386.4:n.1023+28C=
ENST00000321535.4:c.1023+28C=	ENSP00000321386.4:n.1023+28C=
NM_153230.2:c.1023+28C=	NP_694962.1:n.1023+28C=
XM_011523697.1:c.1023+28C=	XP_011521999.1:n.1023+28C=
XR_243544.3:n.1201+28C=
NM_153230.3:c.1023+28C= MANE Select	NP_694962.1:n.1023+28C=