Canonical Allele Identifier: CA3114492

Gene: FGB

Linked Data

• ClinVar Variation Id: 1980460
• ClinVar RCV Id: RCV002761359
• dbSNP Id: rs750691687
• ExAC: 4:155487165 T / TGA
• gnomAD v2: 4-155487165-T-TGA
• gnomAD v3: 4-154566013-T-TGA
• gnomAD v4: 4-154566013-T-TGA
• MyVariant Identifiers: chr4:g.155487165_155487166insGA (hg19) ; chr4:g.154566013_154566014insGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154566014_154566015insAG , CM000666.2:g.154566014_154566015insAG	GRCh38
NC_000004.11:g.155487166_155487167insAG , CM000666.1:g.155487166_155487167insAG	GRCh37
NC_000004.10:g.155706616_155706617insAG	NCBI36
NG_008833.1:g.8035_8036insAG , LRG_558:g.8035_8036insAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000302068.9:c.306+15_306+16insAG MANE Select	ENSP00000306099.4:n.306+15_306+16insAG
ENST00000302068.8:c.306+15_306+16insAG	ENSP00000306099.4:n.306+15_306+16insAG
ENST00000425838.5:c.*218+15_*218+16insAG	ENSP00000398719.1:n.*218+15_*218+16insAG
ENST00000473984.1:n.219+15_219+16insAG
ENST00000497097.5:n.313+15_313+16insAG
ENST00000498375.2:n.936+15_936+16insAG
ENST00000502545.5:n.287+15_287+16insAG
ENST00000509493.1:c.-167-1579_-167-1578insAG	ENSP00000426757.1:n.-167-1579_-167-1578insAG
NM_001184741.1:c.165+156_165+157insAG	NP_001171670.1:n.165+156_165+157insAG
NM_005141.4:c.306+15_306+16insAG , LRG_558t1:c.306+15_306+16insAG	NP_005132.2:n.306+15_306+16insAG
NM_001382759.1:c.306+15_306+16insAG	NP_001369688.1:n.306+15_306+16insAG
NM_001382760.1:c.306+15_306+16insAG	NP_001369689.1:n.306+15_306+16insAG
NM_001382761.1:c.306+15_306+16insAG	NP_001369690.1:n.306+15_306+16insAG
NM_001382762.1:c.306+15_306+16insAG	NP_001369691.1:n.306+15_306+16insAG
NM_001382763.1:c.306+15_306+16insAG	NP_001369692.1:n.306+15_306+16insAG
NM_001382764.1:c.306+15_306+16insAG	NP_001369693.1:n.306+15_306+16insAG
NM_001382765.1:c.306+15_306+16insAG	NP_001369694.1:n.306+15_306+16insAG
NM_005141.5:c.306+15_306+16insAG MANE Select	NP_005132.2:n.306+15_306+16insAG