Canonical Allele Identifier: CA2672440421
Gene: FGB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154565865_154565879del , CM000666.2:g.154565865_154565879del GRCh38
NC_000004.11:g.155487017_155487031del , CM000666.1:g.155487017_155487031del GRCh37
NC_000004.10:g.155706467_155706481del NCBI36
NG_008833.1:g.7886_7900del , LRG_558:g.7886_7900del

Transcript Alleles

HGVS Amino-acid Change
ENST00000302068.9:c.172_186del MANE Select ENSP00000306099.4:p.Ser58_Ala62del
ENST00000302068.8:c.172_186del ENSP00000306099.4:p.Ser58_Ala62del
ENST00000425838.5:c.*84_*98del ENSP00000398719.1:n.*84_*98del
ENST00000473984.1:n.85_99del
ENST00000497097.5:n.179_193del
ENST00000498375.2:n.802_816del
ENST00000502545.5:n.153_167del
ENST00000509493.1:c.-167-1728_-167-1714del ENSP00000426757.1:n.-167-1728_-167-1714del
NM_001184741.1:c.165+7_165+21del NP_001171670.1:n.165+7_165+21del
NM_005141.4:c.172_186del , LRG_558t1:c.172_186del NP_005132.2:p.Ser58_Ala62del
NM_001382759.1:c.172_186del NP_001369688.1:p.Ser58_Ala62del
NM_001382760.1:c.172_186del NP_001369689.1:p.Ser58_Ala62del
NM_001382761.1:c.172_186del NP_001369690.1:p.Ser58_Ala62del
NM_001382762.1:c.172_186del NP_001369691.1:p.Ser58_Ala62del
NM_001382763.1:c.172_186del NP_001369692.1:p.Ser58_Ala62del
NM_001382764.1:c.172_186del NP_001369693.1:p.Ser58_Ala62del
NM_001382765.1:c.172_186del NP_001369694.1:p.Ser58_Ala62del
NM_005141.5:c.172_186del MANE Select NP_005132.2:p.Ser58_Ala62del