Canonical Allele Identifier: CA411329942
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs1230265319
gnomAD v4: 22-32475076-A-G
MyVariant Identifiers: chr22:g.32871063A>G (hg19) chr22:g.32475076A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475076A>G , CM000684.2:g.32475076A>G GRCh38
NC_000022.10:g.32871063A>G , CM000684.1:g.32871063A>G GRCh37
NC_000022.9:g.31201063A>G NCBI36
NG_016001.1:g.5357A>G
NG_016001.2:g.5357A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.74A>G MANE Select ENSP00000266087.7:p.His25Arg
ENST00000266087.11:c.74A>G ENSP00000266087.7:p.His25Arg
ENST00000420700.5:c.74A>G ENSP00000406155.1:p.His25Arg
ENST00000425028.5:c.74A>G ENSP00000395823.1:p.His25Arg
ENST00000492535.1:n.62A>G
NM_012179.3:c.74A>G NP_036311.3:p.His25Arg
XM_011530106.1:c.-100A>G XP_011528408.1:n.-100A>G
XM_024452207.1:c.-117A>G XP_024307975.1:n.-117A>G
NM_012179.4:c.74A>G MANE Select NP_036311.3:p.His25Arg
Search 100 bp 5'
Search 100 bp 3'