Canonical Allele Identifier: CA497690101
Gene: FBXO39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6683805T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780486T>C , CM000679.2:g.6780486T>C GRCh38
NC_000017.10:g.6683805T>C , CM000679.1:g.6683805T>C GRCh37
NC_000017.9:g.6624529T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.618T>C MANE Select ENSP00000321386.4:p.His206=
ENST00000321535.4:c.618T>C ENSP00000321386.4:p.His206=
NM_153230.2:c.618T>C NP_694962.1:p.His206=
XM_011523697.1:c.618T>C XP_011521999.1:p.His206=
XR_243544.3:n.796T>C
NM_153230.3:c.618T>C MANE Select NP_694962.1:p.His206=
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