Canonical Allele Identifier: CA323427796

Gene: FBXO7

Linked Data

• dbSNP Id: rs892014000
• gnomAD v4: 22-32474839-C-G
• MyVariant Identifiers: chr22:g.32870826C>G (hg19) ; chr22:g.32474839C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32474839C>G , CM000684.2:g.32474839C>G	GRCh38
NC_000022.10:g.32870826C>G , CM000684.1:g.32870826C>G	GRCh37
NC_000022.9:g.31200826C>G	NCBI36
NG_016001.1:g.5120C>G
NG_016001.2:g.5120C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.-164C>G MANE Select	ENSP00000266087.7:n.-164C>G
ENST00000266087.11:c.-164C>G	ENSP00000266087.7:n.-164C>G
ENST00000420700.5:c.-164C>G	ENSP00000406155.1:n.-164C>G
ENST00000425028.5:c.-164C>G	ENSP00000395823.1:n.-164C>G
NM_012179.3:c.-164C>G	NP_036311.3:n.-164C>G
XM_011530106.1:c.-337C>G	XP_011528408.1:n.-337C>G
XM_024452207.1:c.-354C>G	XP_024307975.1:n.-354C>G
NM_012179.4:c.-164C>G MANE Select	NP_036311.3:n.-164C>G