Canonical Allele Identifier: CA639098875
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs1407695357
gnomAD v2: 22-32870748-T-G
gnomAD v3: 22-32474761-T-G
gnomAD v4: 22-32474761-T-G
MyVariant Identifiers: chr22:g.32870748T>G (hg19) chr22:g.32474761T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474761T>G , CM000684.2:g.32474761T>G GRCh38
NC_000022.10:g.32870748T>G , CM000684.1:g.32870748T>G GRCh37
NC_000022.9:g.31200748T>G NCBI36
NG_016001.1:g.5042T>G
NG_016001.2:g.5042T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.11:c.-242T>G ENSP00000266087.7:n.-242T>G
ENST00000420700.5:c.-242T>G ENSP00000406155.1:n.-242T>G
NM_012179.3:c.-242T>G NP_036311.3:n.-242T>G
XM_011530106.1:c.-415T>G XP_011528408.1:n.-415T>G
XM_024452207.1:c.-432T>G XP_024307975.1:n.-432T>G
Search 100 bp 5'
Search 100 bp 3'