Canonical Allele Identifier: CA1504935137

Gene: FGB

Linked Data

• ClinVar Variation Id: 2683306
• ClinVar RCV Id: RCV003480126
• dbSNP Id: rs1730132238

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154565827del , CM000666.2:g.154565827del	GRCh38
NC_000004.11:g.155486979del , CM000666.1:g.155486979del	GRCh37
NC_000004.10:g.155706429del	NCBI36
NG_008833.1:g.7848del , LRG_558:g.7848del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.134del MANE Select	ENSP00000306099.4:p.Gly45ValfsTer15
ENST00000302068.8:c.134del	ENSP00000306099.4:p.Gly45ValfsTer15
ENST00000425838.5:c.*46del	ENSP00000398719.1:n.*46del
ENST00000473984.1:n.47del
ENST00000497097.5:n.141del
ENST00000498375.2:n.764del
ENST00000502545.5:n.115del
ENST00000509493.1:c.-167-1766del	ENSP00000426757.1:n.-167-1766del
NM_001184741.1:c.134del	NP_001171670.1:p.Gly45ValfsTer27
NM_005141.4:c.134del , LRG_558t1:c.134del	NP_005132.2:p.Gly45ValfsTer15
NM_001382759.1:c.134del	NP_001369688.1:p.Gly45ValfsTer15
NM_001382760.1:c.134del	NP_001369689.1:p.Gly45ValfsTer15
NM_001382761.1:c.134del	NP_001369690.1:p.Gly45ValfsTer15
NM_001382762.1:c.134del	NP_001369691.1:p.Gly45ValfsTer15
NM_001382763.1:c.134del	NP_001369692.1:p.Gly45ValfsTer15
NM_001382764.1:c.134del	NP_001369693.1:p.Gly45ValfsTer15
NM_001382765.1:c.134del	NP_001369694.1:p.Gly45ValfsTer15
NM_005141.5:c.134del MANE Select	NP_005132.2:p.Gly45ValfsTer15