Canonical Allele Identifier: CA411329861
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs1447013485
MyVariant Identifiers: chr22:g.32871025G>C (hg19) chr22:g.32475038G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475038G>C , CM000684.2:g.32475038G>C GRCh38
NC_000022.10:g.32871025G>C , CM000684.1:g.32871025G>C GRCh37
NC_000022.9:g.31201025G>C NCBI36
NG_016001.1:g.5319G>C
NG_016001.2:g.5319G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.36G>C MANE Select ENSP00000266087.7:p.Trp12Cys
ENST00000266087.11:c.36G>C ENSP00000266087.7:p.Trp12Cys
ENST00000420700.5:c.36G>C ENSP00000406155.1:p.Trp12Cys
ENST00000425028.5:c.36G>C ENSP00000395823.1:p.Trp12Cys
ENST00000492535.1:n.24G>C
NM_012179.3:c.36G>C NP_036311.3:p.Trp12Cys
XM_011530106.1:c.-138G>C XP_011528408.1:n.-138G>C
XM_024452207.1:c.-155G>C XP_024307975.1:n.-155G>C
NM_012179.4:c.36G>C MANE Select NP_036311.3:p.Trp12Cys
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Search 100 bp 3'