Canonical Allele Identifier: CA397763134
Gene: FBXO39 HGNC NCBI

Linked Data

dbSNP Id: rs1221424175
MyVariant Identifiers: chr17:g.6684201C>G (hg19) chr17:g.6780882C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780882C>G , CM000679.2:g.6780882C>G GRCh38
NC_000017.10:g.6684201C>G , CM000679.1:g.6684201C>G GRCh37
NC_000017.9:g.6624925C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.1014C>G MANE Select ENSP00000321386.4:p.His338Gln
ENST00000321535.4:c.1014C>G ENSP00000321386.4:p.His338Gln
NM_153230.2:c.1014C>G NP_694962.1:p.His338Gln
XM_011523697.1:c.1014C>G XP_011521999.1:p.His338Gln
XR_243544.3:n.1192C>G
NM_153230.3:c.1014C>G MANE Select NP_694962.1:p.His338Gln
Search 100 bp 5'
Search 100 bp 3'