Canonical Allele Identifier: CA639098940

Gene: FBXO7

Linked Data

• dbSNP Id: rs1337043616
• gnomAD v2: 22-32870986-C-T
• gnomAD v4: 22-32474999-C-T
• MyVariant Identifiers: chr22:g.32870986C>T (hg19) ; chr22:g.32474999C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32474999C>T , CM000684.2:g.32474999C>T	GRCh38
NC_000022.10:g.32870986C>T , CM000684.1:g.32870986C>T	GRCh37
NC_000022.9:g.31200986C>T	NCBI36
NG_016001.1:g.5280C>T
NG_016001.2:g.5280C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.-4C>T MANE Select	ENSP00000266087.7:n.-4C>T
ENST00000266087.11:c.-4C>T	ENSP00000266087.7:n.-4C>T
ENST00000420700.5:c.-4C>T	ENSP00000406155.1:n.-4C>T
ENST00000425028.5:c.-4C>T	ENSP00000395823.1:n.-4C>T
NM_012179.3:c.-4C>T	NP_036311.3:n.-4C>T
XM_011530106.1:c.-177C>T	XP_011528408.1:n.-177C>T
XM_024452207.1:c.-194C>T	XP_024307975.1:n.-194C>T
NM_012179.4:c.-4C>T MANE Select	NP_036311.3:n.-4C>T