Canonical Allele Identifier: CA774340282
Gene: FBXO39 HGNC NCBI

Linked Data

dbSNP Id: rs1194446237
gnomAD v4: 17-6780901-A-G
MyVariant Identifiers: chr17:g.6684220A>G (hg19) chr17:g.6780901A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780901A>G , CM000679.2:g.6780901A>G GRCh38
NC_000017.10:g.6684220A>G , CM000679.1:g.6684220A>G GRCh37
NC_000017.9:g.6624944A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.1023+10A>G MANE Select ENSP00000321386.4:n.1023+10A>G
ENST00000321535.4:c.1023+10A>G ENSP00000321386.4:n.1023+10A>G
NM_153230.2:c.1023+10A>G NP_694962.1:n.1023+10A>G
XM_011523697.1:c.1023+10A>G XP_011521999.1:n.1023+10A>G
XR_243544.3:n.1201+10A>G
NM_153230.3:c.1023+10A>G MANE Select NP_694962.1:n.1023+10A>G
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