Canonical Allele Identifier: CA1504934979
Gene: FGB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154565619_154565620delinsGT , CM000666.2:g.154565619_154565620delinsGT GRCh38
NC_000004.11:g.155486771_155486772delinsGT , CM000666.1:g.155486771_155486772delinsGT GRCh37
NC_000004.10:g.155706221_155706222delinsGT NCBI36
NG_008833.1:g.7640_7641delinsGT , LRG_558:g.7640_7641delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000302068.9:c.115-189_115-188delinsGT MANE Select ENSP00000306099.4:n.115-189_115-188delinsGT
ENST00000302068.8:c.115-189_115-188delinsGT ENSP00000306099.4:n.115-189_115-188delinsGT
ENST00000425838.5:c.*27-189_*27-188delinsGT ENSP00000398719.1:n.*27-189_*27-188delinsGT
ENST00000497097.5:n.122-189_122-188delinsGT
ENST00000498375.2:n.556_557delinsGT
ENST00000502545.5:n.96-189_96-188delinsGT
ENST00000509493.1:c.-167-1974_-167-1973delinsGT ENSP00000426757.1:n.-167-1974_-167-1973delinsGT
NM_001184741.1:c.115-189_115-188delinsGT NP_001171670.1:n.115-189_115-188delinsGT
NM_005141.4:c.115-189_115-188delinsGT , LRG_558t1:c.115-189_115-188delinsGT NP_005132.2:n.115-189_115-188delinsGT
NM_001382759.1:c.115-189_115-188delinsGT NP_001369688.1:n.115-189_115-188delinsGT
NM_001382760.1:c.115-189_115-188delinsGT NP_001369689.1:n.115-189_115-188delinsGT
NM_001382761.1:c.115-189_115-188delinsGT NP_001369690.1:n.115-189_115-188delinsGT
NM_001382762.1:c.115-189_115-188delinsGT NP_001369691.1:n.115-189_115-188delinsGT
NM_001382763.1:c.115-189_115-188delinsGT NP_001369692.1:n.115-189_115-188delinsGT
NM_001382764.1:c.115-189_115-188delinsGT NP_001369693.1:n.115-189_115-188delinsGT
NM_001382765.1:c.115-189_115-188delinsGT NP_001369694.1:n.115-189_115-188delinsGT
NM_005141.5:c.115-189_115-188delinsGT MANE Select NP_005132.2:n.115-189_115-188delinsGT