Canonical Allele Identifier: CA8332539
Gene: FBXO39 HGNC NCBI

Linked Data

dbSNP Id: rs764959961
ExAC: 17:6684217 A / T
gnomAD v2: 17-6684217-A-T
gnomAD v4: 17-6780898-A-T
MyVariant Identifiers: chr17:g.6684217A>T (hg19) chr17:g.6780898A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780898A>T , CM000679.2:g.6780898A>T GRCh38
NC_000017.10:g.6684217A>T , CM000679.1:g.6684217A>T GRCh37
NC_000017.9:g.6624941A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.1023+7A>T MANE Select ENSP00000321386.4:n.1023+7A>T
ENST00000321535.4:c.1023+7A>T ENSP00000321386.4:n.1023+7A>T
NM_153230.2:c.1023+7A>T NP_694962.1:n.1023+7A>T
XM_011523697.1:c.1023+7A>T XP_011521999.1:n.1023+7A>T
XR_243544.3:n.1201+7A>T
NM_153230.3:c.1023+7A>T MANE Select NP_694962.1:n.1023+7A>T
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