Canonical Allele Identifier: CA2656311098
Gene: FBXO7 HGNC NCBI

Linked Data

gnomAD v4: 22-32474715-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474715T>C , CM000684.2:g.32474715T>C GRCh38
NC_000022.10:g.32870702T>C , CM000684.1:g.32870702T>C GRCh37
NC_000022.9:g.31200702T>C NCBI36
NG_016001.1:g.4996T>C
NG_016001.2:g.4996T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.11:c.-288T>C ENSP00000266087.7:n.-288T>C
ENST00000420700.5:c.-288T>C ENSP00000406155.1:n.-288T>C
XM_011530106.1:c.-461T>C XP_011528408.1:n.-461T>C
XM_024452207.1:c.-478T>C XP_024307975.1:n.-478T>C
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