Canonical Allele Identifier: CA397761940
Gene: FBXO39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6683877C>G (hg19) chr17:g.6780558C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780558C>G , CM000679.2:g.6780558C>G GRCh38
NC_000017.10:g.6683877C>G , CM000679.1:g.6683877C>G GRCh37
NC_000017.9:g.6624601C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.690C>G MANE Select ENSP00000321386.4:p.Asn230Lys
ENST00000321535.4:c.690C>G ENSP00000321386.4:p.Asn230Lys
NM_153230.2:c.690C>G NP_694962.1:p.Asn230Lys
XM_011523697.1:c.690C>G XP_011521999.1:p.Asn230Lys
XR_243544.3:n.868C>G
NM_153230.3:c.690C>G MANE Select NP_694962.1:p.Asn230Lys
Search 100 bp 5'
Search 100 bp 3'