Canonical Allele Identifier: CA2737882999

Gene: FBXO7

Linked Data

• dbSNP Id: rs1408743679

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32474987G>C , CM000684.2:g.32474987G>C	GRCh38
NC_000022.10:g.32870974G>C , CM000684.1:g.32870974G>C	GRCh37
NC_000022.9:g.31200974G>C	NCBI36
NG_016001.1:g.5268G>C
NG_016001.2:g.5268G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.-16G>C MANE Select	ENSP00000266087.7:n.-16G>C
ENST00000266087.11:c.-16G>C	ENSP00000266087.7:n.-16G>C
ENST00000420700.5:c.-16G>C	ENSP00000406155.1:n.-16G>C
ENST00000425028.5:c.-16G>C	ENSP00000395823.1:n.-16G>C
NM_012179.3:c.-16G>C	NP_036311.3:n.-16G>C
XM_011530106.1:c.-189G>C	XP_011528408.1:n.-189G>C
XM_024452207.1:c.-206G>C	XP_024307975.1:n.-206G>C
NM_012179.4:c.-16G>C MANE Select	NP_036311.3:n.-16G>C