Canonical Allele Identifier: CA639098929

Gene: FBXO7

Linked Data

• dbSNP Id: rs756104854
• gnomAD v2: 22-32870967-C-G
• gnomAD v4: 22-32474980-C-G
• MyVariant Identifiers: chr22:g.32870967C>G (hg19) ; chr22:g.32474980C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32474980C>G , CM000684.2:g.32474980C>G	GRCh38
NC_000022.10:g.32870967C>G , CM000684.1:g.32870967C>G	GRCh37
NC_000022.9:g.31200967C>G	NCBI36
NG_016001.1:g.5261C>G
NG_016001.2:g.5261C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000266087.12:c.-23C>G MANE Select	ENSP00000266087.7:n.-23C>G
ENST00000266087.11:c.-23C>G	ENSP00000266087.7:n.-23C>G
ENST00000420700.5:c.-23C>G	ENSP00000406155.1:n.-23C>G
ENST00000425028.5:c.-23C>G	ENSP00000395823.1:n.-23C>G
NM_012179.3:c.-23C>G	NP_036311.3:n.-23C>G
XM_011530106.1:c.-196C>G	XP_011528408.1:n.-196C>G
XM_024452207.1:c.-213C>G	XP_024307975.1:n.-213C>G
NM_012179.4:c.-23C>G MANE Select	NP_036311.3:n.-23C>G