Canonical Allele Identifier: CA497690462
Gene: FBXO39 HGNC NCBI

Linked Data

dbSNP Id: rs777083271
MyVariant Identifiers: chr17:g.6684018C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780699C>G , CM000679.2:g.6780699C>G GRCh38
NC_000017.10:g.6684018C>G , CM000679.1:g.6684018C>G GRCh37
NC_000017.9:g.6624742C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.831C>G MANE Select ENSP00000321386.4:p.Ala277=
ENST00000321535.4:c.831C>G ENSP00000321386.4:p.Ala277=
NM_153230.2:c.831C>G NP_694962.1:p.Ala277=
XM_011523697.1:c.831C>G XP_011521999.1:p.Ala277=
XR_243544.3:n.1009C>G
NM_153230.3:c.831C>G MANE Select NP_694962.1:p.Ala277=
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