Canonical Allele Identifier: CA2672440446

Gene: FGB

Linked Data

• gnomAD v4: 4-154565897-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154565899del , CM000666.2:g.154565899del	GRCh38
NC_000004.11:g.155487051del , CM000666.1:g.155487051del	GRCh37
NC_000004.10:g.155706501del	NCBI36
NG_008833.1:g.7920del , LRG_558:g.7920del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.206del MANE Select	ENSP00000306099.4:p.Gly69ValfsTer17
ENST00000302068.8:c.206del	ENSP00000306099.4:p.Gly69ValfsTer17
ENST00000425838.5:c.*118del	ENSP00000398719.1:n.*118del
ENST00000473984.1:n.119del
ENST00000497097.5:n.213del
ENST00000498375.2:n.836del
ENST00000502545.5:n.187del
ENST00000509493.1:c.-167-1694del	ENSP00000426757.1:n.-167-1694del
NM_001184741.1:c.165+41del	NP_001171670.1:n.165+41del
NM_005141.4:c.206del , LRG_558t1:c.206del	NP_005132.2:p.Gly69ValfsTer17
NM_001382759.1:c.206del	NP_001369688.1:p.Gly69ValfsTer17
NM_001382760.1:c.206del	NP_001369689.1:p.Gly69ValfsTer17
NM_001382761.1:c.206del	NP_001369690.1:p.Gly69ValfsTer17
NM_001382762.1:c.206del	NP_001369691.1:p.Gly69ValfsTer17
NM_001382763.1:c.206del	NP_001369692.1:p.Gly69ValfsTer17
NM_001382764.1:c.206del	NP_001369693.1:p.Gly69ValfsTer17
NM_001382765.1:c.206del	NP_001369694.1:p.Gly69ValfsTer17
NM_005141.5:c.206del MANE Select	NP_005132.2:p.Gly69ValfsTer17