Canonical Allele Identifier: CA397761413
Gene: FBXO39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6683786T>G (hg19) chr17:g.6780467T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780467T>G , CM000679.2:g.6780467T>G GRCh38
NC_000017.10:g.6683786T>G , CM000679.1:g.6683786T>G GRCh37
NC_000017.9:g.6624510T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.599T>G MANE Select ENSP00000321386.4:p.Ile200Ser
ENST00000321535.4:c.599T>G ENSP00000321386.4:p.Ile200Ser
NM_153230.2:c.599T>G NP_694962.1:p.Ile200Ser
XM_011523697.1:c.599T>G XP_011521999.1:p.Ile200Ser
XR_243544.3:n.777T>G
NM_153230.3:c.599T>G MANE Select NP_694962.1:p.Ile200Ser
Search 100 bp 5'
Search 100 bp 3'