Canonical Allele Identifier: CA497690154
Gene: FBXO39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6683874G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780555G>C , CM000679.2:g.6780555G>C GRCh38
NC_000017.10:g.6683874G>C , CM000679.1:g.6683874G>C GRCh37
NC_000017.9:g.6624598G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.687G>C MANE Select ENSP00000321386.4:p.Leu229=
ENST00000321535.4:c.687G>C ENSP00000321386.4:p.Leu229=
NM_153230.2:c.687G>C NP_694962.1:p.Leu229=
XM_011523697.1:c.687G>C XP_011521999.1:p.Leu229=
XR_243544.3:n.865G>C
NM_153230.3:c.687G>C MANE Select NP_694962.1:p.Leu229=