Canonical Allele Identifier: CA639098963
Gene: FBXO7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2994368
ClinVar RCV Id: RCV003856007
dbSNP Id: rs1258057988
gnomAD v2: 22-32871128-G-A
gnomAD v3: 22-32475141-G-A
gnomAD v4: 22-32475141-G-A
MyVariant Identifiers: chr22:g.32871128G>A (hg19) chr22:g.32475141G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475141G>A , CM000684.2:g.32475141G>A GRCh38
NC_000022.10:g.32871128G>A , CM000684.1:g.32871128G>A GRCh37
NC_000022.9:g.31201128G>A NCBI36
NG_016001.1:g.5422G>A
NG_016001.2:g.5422G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.122+17G>A MANE Select ENSP00000266087.7:n.122+17G>A
ENST00000266087.11:c.122+17G>A ENSP00000266087.7:n.122+17G>A
ENST00000420700.5:c.122+17G>A ENSP00000406155.1:n.122+17G>A
ENST00000425028.5:c.122+17G>A ENSP00000395823.1:n.122+17G>A
ENST00000492535.1:n.110+17G>A
NM_012179.3:c.122+17G>A NP_036311.3:n.122+17G>A
XM_011530106.1:c.-52+17G>A XP_011528408.1:n.-52+17G>A
XM_024452207.1:c.-69+17G>A XP_024307975.1:n.-69+17G>A
NM_012179.4:c.122+17G>A MANE Select NP_036311.3:n.122+17G>A
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