Canonical Allele Identifier: CA558056207

Gene: FBXL7

Linked Data

• dbSNP Id: rs1478693752
• gnomAD v2: 5-15783673-A-G
• gnomAD v3: 5-15783564-A-G
• gnomAD v4: 5-15783564-A-G
• MyVariant Identifiers: chr5:g.15783673A>G (hg19) ; chr5:g.15783564A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.15783564A>G , CM000667.2:g.15783564A>G	GRCh38
NC_000005.9:g.15783673A>G , CM000667.1:g.15783673A>G	GRCh37
NC_000005.8:g.15836673A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504595.2:c.128-144326A>G MANE Select	ENSP00000423630.1:n.128-144326A>G
ENST00000504595.1:c.128-144326A>G	ENSP00000423630.1:n.128-144326A>G
ENST00000510662.1:c.-14-144326A>G	ENSP00000425184.1:n.-14-144326A>G
NM_001278317.1:c.-14-144326A>G	NP_001265246.1:n.-14-144326A>G
NM_012304.4:c.128-144326A>G	NP_036436.1:n.128-144326A>G
XM_005248273.3:c.113-144326A>G	XP_005248330.1:n.113-144326A>G
XM_011513998.1:c.-91-51213A>G	XP_011512300.1:n.-91-51213A>G
XM_017009262.2:c.113-144326A>G	XP_016864751.1:n.113-144326A>G
NM_012304.5:c.128-144326A>G MANE Select	NP_036436.1:n.128-144326A>G
NM_001278317.2:c.-14-144326A>G	NP_001265246.1:n.-14-144326A>G