Canonical Allele Identifier: CA10201288

Gene: FBXO7

Linked Data

• dbSNP Id: rs779932728
• ExAC: 22:32870977 G / T
• gnomAD v2: 22-32870977-G-T
• gnomAD v3: 22-32474990-G-T
• gnomAD v4: 22-32474990-G-T
• MyVariant Identifiers: chr22:g.32870977G>T (hg19) ; chr22:g.32474990G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32474990G>T , CM000684.2:g.32474990G>T	GRCh38
NC_000022.10:g.32870977G>T , CM000684.1:g.32870977G>T	GRCh37
NC_000022.9:g.31200977G>T	NCBI36
NG_016001.1:g.5271G>T
NG_016001.2:g.5271G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.-13G>T MANE Select	ENSP00000266087.7:n.-13G>T
ENST00000266087.11:c.-13G>T	ENSP00000266087.7:n.-13G>T
ENST00000420700.5:c.-13G>T	ENSP00000406155.1:n.-13G>T
ENST00000425028.5:c.-13G>T	ENSP00000395823.1:n.-13G>T
NM_012179.3:c.-13G>T	NP_036311.3:n.-13G>T
XM_011530106.1:c.-186G>T	XP_011528408.1:n.-186G>T
XM_024452207.1:c.-203G>T	XP_024307975.1:n.-203G>T
NM_012179.4:c.-13G>T MANE Select	NP_036311.3:n.-13G>T