Canonical Allele Identifier: CA397762641
Gene: FBXO39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6684121A>C (hg19) chr17:g.6780802A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780802A>C , CM000679.2:g.6780802A>C GRCh38
NC_000017.10:g.6684121A>C , CM000679.1:g.6684121A>C GRCh37
NC_000017.9:g.6624845A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.934A>C MANE Select ENSP00000321386.4:p.Ser312Arg
ENST00000321535.4:c.934A>C ENSP00000321386.4:p.Ser312Arg
NM_153230.2:c.934A>C NP_694962.1:p.Ser312Arg
XM_011523697.1:c.934A>C XP_011521999.1:p.Ser312Arg
XR_243544.3:n.1112A>C
NM_153230.3:c.934A>C MANE Select NP_694962.1:p.Ser312Arg
Search 100 bp 5'
Search 100 bp 3'