Canonical Allele Identifier: CA323427682
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs775629881
gnomAD v2: 22-32870673-G-A
gnomAD v3: 22-32474686-G-A
gnomAD v4: 22-32474686-G-A
MyVariant Identifiers: chr22:g.32870673G>A (hg19) chr22:g.32474686G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474686G>A , CM000684.2:g.32474686G>A GRCh38
NC_000022.10:g.32870673G>A , CM000684.1:g.32870673G>A GRCh37
NC_000022.9:g.31200673G>A NCBI36
NG_016001.1:g.4967G>A
NG_016001.2:g.4967G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.11:c.-317G>A ENSP00000266087.7:n.-317G>A
ENST00000420700.5:c.-317G>A ENSP00000406155.1:n.-317G>A
XM_011530106.1:c.-490G>A XP_011528408.1:n.-490G>A
XM_024452207.1:c.-507G>A XP_024307975.1:n.-507G>A
Search 100 bp 5'
Search 100 bp 3'