Canonical Allele Identifier: CA789366795

Gene: FGB

Linked Data

• dbSNP Id: rs1215431133
• MyVariant Identifiers: chr4:g.155486772del (hg19) ; chr4:g.154565620del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154565621del , CM000666.2:g.154565621del	GRCh38
NC_000004.11:g.155486773del , CM000666.1:g.155486773del	GRCh37
NC_000004.10:g.155706223del	NCBI36
NG_008833.1:g.7642del , LRG_558:g.7642del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.115-187del MANE Select	ENSP00000306099.4:n.115-187del
ENST00000302068.8:c.115-187del	ENSP00000306099.4:n.115-187del
ENST00000425838.5:c.*27-187del	ENSP00000398719.1:n.*27-187del
ENST00000497097.5:n.122-187del
ENST00000498375.2:n.558del
ENST00000502545.5:n.96-187del
ENST00000509493.1:c.-167-1972del	ENSP00000426757.1:n.-167-1972del
NM_001184741.1:c.115-187del	NP_001171670.1:n.115-187del
NM_005141.4:c.115-187del , LRG_558t1:c.115-187del	NP_005132.2:n.115-187del
NM_001382759.1:c.115-187del	NP_001369688.1:n.115-187del
NM_001382760.1:c.115-187del	NP_001369689.1:n.115-187del
NM_001382761.1:c.115-187del	NP_001369690.1:n.115-187del
NM_001382762.1:c.115-187del	NP_001369691.1:n.115-187del
NM_001382763.1:c.115-187del	NP_001369692.1:n.115-187del
NM_001382764.1:c.115-187del	NP_001369693.1:n.115-187del
NM_001382765.1:c.115-187del	NP_001369694.1:n.115-187del
NM_005141.5:c.115-187del MANE Select	NP_005132.2:n.115-187del