Canonical Allele Identifier: CA639098931

Gene: FBXO7

Linked Data

• dbSNP Id: rs1162769291
• gnomAD v2: 22-32870969-C-G
• gnomAD v4: 22-32474982-C-G
• MyVariant Identifiers: chr22:g.32870969C>G (hg19) ; chr22:g.32474982C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32474982C>G , CM000684.2:g.32474982C>G	GRCh38
NC_000022.10:g.32870969C>G , CM000684.1:g.32870969C>G	GRCh37
NC_000022.9:g.31200969C>G	NCBI36
NG_016001.1:g.5263C>G
NG_016001.2:g.5263C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000266087.12:c.-21C>G MANE Select	ENSP00000266087.7:n.-21C>G
ENST00000266087.11:c.-21C>G	ENSP00000266087.7:n.-21C>G
ENST00000420700.5:c.-21C>G	ENSP00000406155.1:n.-21C>G
ENST00000425028.5:c.-21C>G	ENSP00000395823.1:n.-21C>G
NM_012179.3:c.-21C>G	NP_036311.3:n.-21C>G
XM_011530106.1:c.-194C>G	XP_011528408.1:n.-194C>G
XM_024452207.1:c.-211C>G	XP_024307975.1:n.-211C>G
NM_012179.4:c.-21C>G MANE Select	NP_036311.3:n.-21C>G