Canonical Allele Identifier: CA2672439831
Gene: FGB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154565507_154565508insCA , CM000666.2:g.154565507_154565508insCA GRCh38
NC_000004.11:g.155486659_155486660insCA , CM000666.1:g.155486659_155486660insCA GRCh37
NC_000004.10:g.155706109_155706110insCA NCBI36
NG_008833.1:g.7528_7529insCA , LRG_558:g.7528_7529insCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000302068.9:c.115-301_115-300insCA MANE Select ENSP00000306099.4:n.115-301_115-300insCA
ENST00000302068.8:c.115-301_115-300insCA ENSP00000306099.4:n.115-301_115-300insCA
ENST00000425838.5:c.*26+272_*26+273insCA ENSP00000398719.1:n.*26+272_*26+273insCA
ENST00000497097.5:n.122-301_122-300insCA
ENST00000498375.2:n.444_445insCA
ENST00000502545.5:n.96-301_96-300insCA
ENST00000509493.1:c.-167-2086_-167-2085insCA ENSP00000426757.1:n.-167-2086_-167-2085insCA
NM_001184741.1:c.115-301_115-300insCA NP_001171670.1:n.115-301_115-300insCA
NM_005141.4:c.115-301_115-300insCA , LRG_558t1:c.115-301_115-300insCA NP_005132.2:n.115-301_115-300insCA
NM_001382759.1:c.115-301_115-300insCA NP_001369688.1:n.115-301_115-300insCA
NM_001382760.1:c.115-301_115-300insCA NP_001369689.1:n.115-301_115-300insCA
NM_001382761.1:c.115-301_115-300insCA NP_001369690.1:n.115-301_115-300insCA
NM_001382762.1:c.115-301_115-300insCA NP_001369691.1:n.115-301_115-300insCA
NM_001382763.1:c.115-301_115-300insCA NP_001369692.1:n.115-301_115-300insCA
NM_001382764.1:c.115-301_115-300insCA NP_001369693.1:n.115-301_115-300insCA
NM_001382765.1:c.115-301_115-300insCA NP_001369694.1:n.115-301_115-300insCA
NM_005141.5:c.115-301_115-300insCA MANE Select NP_005132.2:n.115-301_115-300insCA