Canonical Allele Identifier: CA514294306
Gene: FBXO7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2892454
ClinVar RCV Id: RCV003611478
gnomAD v4: 22-32475035-C-G
MyVariant Identifiers: chr22:g.32871022C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475035C>G , CM000684.2:g.32475035C>G GRCh38
NC_000022.10:g.32871022C>G , CM000684.1:g.32871022C>G GRCh37
NC_000022.9:g.31201022C>G NCBI36
NG_016001.1:g.5316C>G
NG_016001.2:g.5316C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.33C>G MANE Select ENSP00000266087.7:p.Thr11=
ENST00000266087.11:c.33C>G ENSP00000266087.7:p.Thr11=
ENST00000420700.5:c.33C>G ENSP00000406155.1:p.Thr11=
ENST00000425028.5:c.33C>G ENSP00000395823.1:p.Thr11=
ENST00000492535.1:n.21C>G
NM_012179.3:c.33C>G NP_036311.3:p.Thr11=
XM_011530106.1:c.-141C>G XP_011528408.1:n.-141C>G
XM_024452207.1:c.-158C>G XP_024307975.1:n.-158C>G
NM_012179.4:c.33C>G MANE Select NP_036311.3:p.Thr11=
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