Canonical Allele Identifier: CA10653375
Gene: FBXO7 HGNC NCBI

Linked Data

ClinVar Variation Id: 341300
ClinVar RCV Id: RCV000334060
dbSNP Id: rs886057415
gnomAD v3: 22-32474803-G-A
gnomAD v4: 22-32474803-G-A
MyVariant Identifiers: chr22:g.32870790G>A (hg19) chr22:g.32474803G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474803G>A , CM000684.2:g.32474803G>A GRCh38
NC_000022.10:g.32870790G>A , CM000684.1:g.32870790G>A GRCh37
NC_000022.9:g.31200790G>A NCBI36
NG_016001.1:g.5084G>A
NG_016001.2:g.5084G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.11:c.-200G>A ENSP00000266087.7:n.-200G>A
ENST00000420700.5:c.-200G>A ENSP00000406155.1:n.-200G>A
ENST00000425028.5:c.-200G>A ENSP00000395823.1:n.-200G>A
NM_012179.3:c.-200G>A NP_036311.3:n.-200G>A
XM_011530106.1:c.-373G>A XP_011528408.1:n.-373G>A
XM_024452207.1:c.-390G>A XP_024307975.1:n.-390G>A
Search 100 bp 5'
Search 100 bp 3'