Canonical Allele Identifier: CA2672440004

Gene: FGB

Linked Data

• gnomAD v4: 4-154565615-TGCAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154565616_154565619del , CM000666.2:g.154565616_154565619del	GRCh38
NC_000004.11:g.155486768_155486771del , CM000666.1:g.155486768_155486771del	GRCh37
NC_000004.10:g.155706218_155706221del	NCBI36
NG_008833.1:g.7637_7640del , LRG_558:g.7637_7640del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.115-192_115-189del MANE Select	ENSP00000306099.4:n.115-192_115-189del
ENST00000302068.8:c.115-192_115-189del	ENSP00000306099.4:n.115-192_115-189del
ENST00000425838.5:c.*27-192_*27-189del	ENSP00000398719.1:n.*27-192_*27-189del
ENST00000497097.5:n.122-192_122-189del
ENST00000498375.2:n.553_556del
ENST00000502545.5:n.96-192_96-189del
ENST00000509493.1:c.-167-1977_-167-1974del	ENSP00000426757.1:n.-167-1977_-167-1974del
NM_001184741.1:c.115-192_115-189del	NP_001171670.1:n.115-192_115-189del
NM_005141.4:c.115-192_115-189del , LRG_558t1:c.115-192_115-189del	NP_005132.2:n.115-192_115-189del
NM_001382759.1:c.115-192_115-189del	NP_001369688.1:n.115-192_115-189del
NM_001382760.1:c.115-192_115-189del	NP_001369689.1:n.115-192_115-189del
NM_001382761.1:c.115-192_115-189del	NP_001369690.1:n.115-192_115-189del
NM_001382762.1:c.115-192_115-189del	NP_001369691.1:n.115-192_115-189del
NM_001382763.1:c.115-192_115-189del	NP_001369692.1:n.115-192_115-189del
NM_001382764.1:c.115-192_115-189del	NP_001369693.1:n.115-192_115-189del
NM_001382765.1:c.115-192_115-189del	NP_001369694.1:n.115-192_115-189del
NM_005141.5:c.115-192_115-189del MANE Select	NP_005132.2:n.115-192_115-189del