Canonical Allele Identifier: CA397763148
Gene: FBXO39 HGNC NCBI

Linked Data

dbSNP Id: rs1452719497
MyVariant Identifiers: chr17:g.6684203C>T (hg19) chr17:g.6780884C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780884C>T , CM000679.2:g.6780884C>T GRCh38
NC_000017.10:g.6684203C>T , CM000679.1:g.6684203C>T GRCh37
NC_000017.9:g.6624927C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.1016C>T MANE Select ENSP00000321386.4:p.Thr339Ile
ENST00000321535.4:c.1016C>T ENSP00000321386.4:p.Thr339Ile
NM_153230.2:c.1016C>T NP_694962.1:p.Thr339Ile
XM_011523697.1:c.1016C>T XP_011521999.1:p.Thr339Ile
XR_243544.3:n.1194C>T
NM_153230.3:c.1016C>T MANE Select NP_694962.1:p.Thr339Ile
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