Canonical Allele Identifier: CA1073534218

Gene: FBXL7

Linked Data

• dbSNP Id: rs1737056582
• gnomAD v3: 5-15783594-G-C
• gnomAD v4: 5-15783594-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.15783594G>C , CM000667.2:g.15783594G>C	GRCh38
NC_000005.9:g.15783703G>C , CM000667.1:g.15783703G>C	GRCh37
NC_000005.8:g.15836703G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504595.2:c.128-144296G>C MANE Select	ENSP00000423630.1:n.128-144296G>C
ENST00000504595.1:c.128-144296G>C	ENSP00000423630.1:n.128-144296G>C
ENST00000510662.1:c.-14-144296G>C	ENSP00000425184.1:n.-14-144296G>C
NM_001278317.1:c.-14-144296G>C	NP_001265246.1:n.-14-144296G>C
NM_012304.4:c.128-144296G>C	NP_036436.1:n.128-144296G>C
XM_005248273.3:c.113-144296G>C	XP_005248330.1:n.113-144296G>C
XM_011513998.1:c.-91-51183G>C	XP_011512300.1:n.-91-51183G>C
XM_017009262.2:c.113-144296G>C	XP_016864751.1:n.113-144296G>C
NM_012304.5:c.128-144296G>C MANE Select	NP_036436.1:n.128-144296G>C
NM_001278317.2:c.-14-144296G>C	NP_001265246.1:n.-14-144296G>C