Canonical Allele Identifier: CA752546036

Gene: FBXO7

Linked Data

• dbSNP Id: rs1361051461
• gnomAD v3: 22-32474955-C-T
• gnomAD v4: 22-32474955-C-T
• MyVariant Identifiers: chr22:g.32870942C>T (hg19) ; chr22:g.32474955C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32474955C>T , CM000684.2:g.32474955C>T	GRCh38
NC_000022.10:g.32870942C>T , CM000684.1:g.32870942C>T	GRCh37
NC_000022.9:g.31200942C>T	NCBI36
NG_016001.1:g.5236C>T
NG_016001.2:g.5236C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.-48C>T MANE Select	ENSP00000266087.7:n.-48C>T
ENST00000266087.11:c.-48C>T	ENSP00000266087.7:n.-48C>T
ENST00000420700.5:c.-48C>T	ENSP00000406155.1:n.-48C>T
ENST00000425028.5:c.-48C>T	ENSP00000395823.1:n.-48C>T
NM_012179.3:c.-48C>T	NP_036311.3:n.-48C>T
XM_011530106.1:c.-221C>T	XP_011528408.1:n.-221C>T
XM_024452207.1:c.-238C>T	XP_024307975.1:n.-238C>T
NM_012179.4:c.-48C>T MANE Select	NP_036311.3:n.-48C>T