Canonical Allele Identifier: CA639098902

Gene: FBXO7

Linked Data

• dbSNP Id: rs1412316756
• gnomAD v2: 22-32870907-G-C
• gnomAD v3: 22-32474920-G-C
• gnomAD v4: 22-32474920-G-C
• MyVariant Identifiers: chr22:g.32870907G>C (hg19) ; chr22:g.32474920G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32474920G>C , CM000684.2:g.32474920G>C	GRCh38
NC_000022.10:g.32870907G>C , CM000684.1:g.32870907G>C	GRCh37
NC_000022.9:g.31200907G>C	NCBI36
NG_016001.1:g.5201G>C
NG_016001.2:g.5201G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.-83G>C MANE Select	ENSP00000266087.7:n.-83G>C
ENST00000266087.11:c.-83G>C	ENSP00000266087.7:n.-83G>C
ENST00000420700.5:c.-83G>C	ENSP00000406155.1:n.-83G>C
ENST00000425028.5:c.-83G>C	ENSP00000395823.1:n.-83G>C
NM_012179.3:c.-83G>C	NP_036311.3:n.-83G>C
XM_011530106.1:c.-256G>C	XP_011528408.1:n.-256G>C
XM_024452207.1:c.-273G>C	XP_024307975.1:n.-273G>C
NM_012179.4:c.-83G>C MANE Select	NP_036311.3:n.-83G>C