Canonical Allele Identifier: CA397762492
Gene: FBXO39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6684062T>C (hg19) chr17:g.6780743T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780743T>C , CM000679.2:g.6780743T>C GRCh38
NC_000017.10:g.6684062T>C , CM000679.1:g.6684062T>C GRCh37
NC_000017.9:g.6624786T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.875T>C MANE Select ENSP00000321386.4:p.Ile292Thr
ENST00000321535.4:c.875T>C ENSP00000321386.4:p.Ile292Thr
NM_153230.2:c.875T>C NP_694962.1:p.Ile292Thr
XM_011523697.1:c.875T>C XP_011521999.1:p.Ile292Thr
XR_243544.3:n.1053T>C
NM_153230.3:c.875T>C MANE Select NP_694962.1:p.Ile292Thr
Search 100 bp 5'
Search 100 bp 3'