Canonical Allele Identifier: CA397761838
Gene: FBXO39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6683857C>G (hg19) chr17:g.6780538C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780538C>G , CM000679.2:g.6780538C>G GRCh38
NC_000017.10:g.6683857C>G , CM000679.1:g.6683857C>G GRCh37
NC_000017.9:g.6624581C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.670C>G MANE Select ENSP00000321386.4:p.His224Asp
ENST00000321535.4:c.670C>G ENSP00000321386.4:p.His224Asp
NM_153230.2:c.670C>G NP_694962.1:p.His224Asp
XM_011523697.1:c.670C>G XP_011521999.1:p.His224Asp
XR_243544.3:n.848C>G
NM_153230.3:c.670C>G MANE Select NP_694962.1:p.His224Asp
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