Canonical Allele Identifier: CA323427870

Gene: FBXO7

Linked Data

• dbSNP Id: rs916933836
• MyVariant Identifiers: chr22:g.32870968C>T (hg19) ; chr22:g.32474981C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32474981C>T , CM000684.2:g.32474981C>T	GRCh38
NC_000022.10:g.32870968C>T , CM000684.1:g.32870968C>T	GRCh37
NC_000022.9:g.31200968C>T	NCBI36
NG_016001.1:g.5262C>T
NG_016001.2:g.5262C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000266087.12:c.-22C>T MANE Select	ENSP00000266087.7:n.-22C>T
ENST00000266087.11:c.-22C>T	ENSP00000266087.7:n.-22C>T
ENST00000420700.5:c.-22C>T	ENSP00000406155.1:n.-22C>T
ENST00000425028.5:c.-22C>T	ENSP00000395823.1:n.-22C>T
NM_012179.3:c.-22C>T	NP_036311.3:n.-22C>T
XM_011530106.1:c.-195C>T	XP_011528408.1:n.-195C>T
XM_024452207.1:c.-212C>T	XP_024307975.1:n.-212C>T
NM_012179.4:c.-22C>T MANE Select	NP_036311.3:n.-22C>T