Canonical Allele Identifier: CA639098871
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs974764171
gnomAD v2: 22-32870736-C-G
gnomAD v3: 22-32474749-C-G
gnomAD v4: 22-32474749-C-G
MyVariant Identifiers: chr22:g.32870736C>G (hg19) chr22:g.32474749C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474749C>G , CM000684.2:g.32474749C>G GRCh38
NC_000022.10:g.32870736C>G , CM000684.1:g.32870736C>G GRCh37
NC_000022.9:g.31200736C>G NCBI36
NG_016001.1:g.5030C>G
NG_016001.2:g.5030C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.11:c.-254C>G ENSP00000266087.7:n.-254C>G
ENST00000420700.5:c.-254C>G ENSP00000406155.1:n.-254C>G
NM_012179.3:c.-254C>G NP_036311.3:n.-254C>G
XM_011530106.1:c.-427C>G XP_011528408.1:n.-427C>G
XM_024452207.1:c.-444C>G XP_024307975.1:n.-444C>G
Search 100 bp 5'
Search 100 bp 3'