Canonical Allele Identifier: CA10654048
Gene: FBXO7 HGNC NCBI

Linked Data

ClinVar Variation Id: 341304
ClinVar RCV Id: RCV000375116
dbSNP Id: rs886057418
gnomAD v4: 22-32474885-T-G
MyVariant Identifiers: chr22:g.32870872T>G (hg19) chr22:g.32474885T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474885T>G , CM000684.2:g.32474885T>G GRCh38
NC_000022.10:g.32870872T>G , CM000684.1:g.32870872T>G GRCh37
NC_000022.9:g.31200872T>G NCBI36
NG_016001.1:g.5166T>G
NG_016001.2:g.5166T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.-118T>G MANE Select ENSP00000266087.7:n.-118T>G
ENST00000266087.11:c.-118T>G ENSP00000266087.7:n.-118T>G
ENST00000420700.5:c.-118T>G ENSP00000406155.1:n.-118T>G
ENST00000425028.5:c.-118T>G ENSP00000395823.1:n.-118T>G
NM_012179.3:c.-118T>G NP_036311.3:n.-118T>G
XM_011530106.1:c.-291T>G XP_011528408.1:n.-291T>G
XM_024452207.1:c.-308T>G XP_024307975.1:n.-308T>G
NM_012179.4:c.-118T>G MANE Select NP_036311.3:n.-118T>G
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