Canonical Allele Identifier: CA323427859

Gene: FBXO7

Linked Data

• dbSNP Id: rs1050237991
• gnomAD v3: 22-32474941-G-C
• gnomAD v4: 22-32474941-G-C
• MyVariant Identifiers: chr22:g.32870928G>C (hg19) ; chr22:g.32474941G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32474941G>C , CM000684.2:g.32474941G>C	GRCh38
NC_000022.10:g.32870928G>C , CM000684.1:g.32870928G>C	GRCh37
NC_000022.9:g.31200928G>C	NCBI36
NG_016001.1:g.5222G>C
NG_016001.2:g.5222G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.-62G>C MANE Select	ENSP00000266087.7:n.-62G>C
ENST00000266087.11:c.-62G>C	ENSP00000266087.7:n.-62G>C
ENST00000420700.5:c.-62G>C	ENSP00000406155.1:n.-62G>C
ENST00000425028.5:c.-62G>C	ENSP00000395823.1:n.-62G>C
NM_012179.3:c.-62G>C	NP_036311.3:n.-62G>C
XM_011530106.1:c.-235G>C	XP_011528408.1:n.-235G>C
XM_024452207.1:c.-252G>C	XP_024307975.1:n.-252G>C
NM_012179.4:c.-62G>C MANE Select	NP_036311.3:n.-62G>C