Canonical Allele Identifier: CA2401985156

Gene: FBXO7

Linked Data

• dbSNP Id: rs2057416095

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32474959T>C , CM000684.2:g.32474959T>C	GRCh38
NC_000022.10:g.32870946T>C , CM000684.1:g.32870946T>C	GRCh37
NC_000022.9:g.31200946T>C	NCBI36
NG_016001.1:g.5240T>C
NG_016001.2:g.5240T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.-44T>C MANE Select	ENSP00000266087.7:n.-44T>C
ENST00000266087.11:c.-44T>C	ENSP00000266087.7:n.-44T>C
ENST00000420700.5:c.-44T>C	ENSP00000406155.1:n.-44T>C
ENST00000425028.5:c.-44T>C	ENSP00000395823.1:n.-44T>C
NM_012179.3:c.-44T>C	NP_036311.3:n.-44T>C
XM_011530106.1:c.-217T>C	XP_011528408.1:n.-217T>C
XM_024452207.1:c.-234T>C	XP_024307975.1:n.-234T>C
NM_012179.4:c.-44T>C MANE Select	NP_036311.3:n.-44T>C