Canonical Allele Identifier: CA2840156960

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154565888_154565889insTG , CM000666.2:g.154565888_154565889insTG	GRCh38
NC_000004.11:g.155487040_155487041insTG , CM000666.1:g.155487040_155487041insTG	GRCh37
NC_000004.10:g.155706490_155706491insTG	NCBI36
NG_008833.1:g.7909_7910insTG , LRG_558:g.7909_7910insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.195_196insTG MANE Select	ENSP00000306099.4:p.Ile66Ter
ENST00000302068.8:c.195_196insTG	ENSP00000306099.4:p.Ile66Ter
ENST00000425838.5:c.*107_*108insTG	ENSP00000398719.1:n.*107_*108insTG
ENST00000473984.1:n.108_109insTG
ENST00000497097.5:n.202_203insTG
ENST00000498375.2:n.825_826insTG
ENST00000502545.5:n.176_177insTG
ENST00000509493.1:c.-167-1705_-167-1704insTG	ENSP00000426757.1:n.-167-1705_-167-1704insTG
NM_001184741.1:c.165+30_165+31insTG	NP_001171670.1:n.165+30_165+31insTG
NM_005141.4:c.195_196insTG , LRG_558t1:c.195_196insTG	NP_005132.2:p.Ile66Ter
NM_001382759.1:c.195_196insTG	NP_001369688.1:p.Ile66Ter
NM_001382760.1:c.195_196insTG	NP_001369689.1:p.Ile66Ter
NM_001382761.1:c.195_196insTG	NP_001369690.1:p.Ile66Ter
NM_001382762.1:c.195_196insTG	NP_001369691.1:p.Ile66Ter
NM_001382763.1:c.195_196insTG	NP_001369692.1:p.Ile66Ter
NM_001382764.1:c.195_196insTG	NP_001369693.1:p.Ile66Ter
NM_001382765.1:c.195_196insTG	NP_001369694.1:p.Ile66Ter
NM_005141.5:c.195_196insTG MANE Select	NP_005132.2:p.Ile66Ter