Canonical Allele Identifier: CA2401984955
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs1450012741
gnomAD v4: 22-32474677-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474677G>C , CM000684.2:g.32474677G>C GRCh38
NC_000022.10:g.32870664G>C , CM000684.1:g.32870664G>C GRCh37
NC_000022.9:g.31200664G>C NCBI36
NG_016001.1:g.4958G>C
NG_016001.2:g.4958G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.11:c.-326G>C ENSP00000266087.7:n.-326G>C
ENST00000420700.5:c.-326G>C ENSP00000406155.1:n.-326G>C
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