Canonical Allele Identifier: CA1504935099

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154565796C= , CM000666.2:g.154565796C=	GRCh38
NC_000004.11:g.155486948C= , CM000666.1:g.155486948C=	GRCh37
NC_000004.10:g.155706398C=	NCBI36
NG_008833.1:g.7817C= , LRG_558:g.7817C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.115-12C= MANE Select	ENSP00000306099.4:n.115-12C=
ENST00000302068.8:c.115-12C=	ENSP00000306099.4:n.115-12C=
ENST00000425838.5:c.*27-12C=	ENSP00000398719.1:n.*27-12C=
ENST00000473984.1:n.16C=
ENST00000497097.5:n.122-12C=
ENST00000498375.2:n.733C=
ENST00000502545.5:n.96-12C=
ENST00000509493.1:c.-167-1797C=	ENSP00000426757.1:n.-167-1797C=
NM_001184741.1:c.115-12C=	NP_001171670.1:n.115-12C=
NM_005141.4:c.115-12C= , LRG_558t1:c.115-12C=	NP_005132.2:n.115-12C=
NM_001382759.1:c.115-12C=	NP_001369688.1:n.115-12C=
NM_001382760.1:c.115-12C=	NP_001369689.1:n.115-12C=
NM_001382761.1:c.115-12C=	NP_001369690.1:n.115-12C=
NM_001382762.1:c.115-12C=	NP_001369691.1:n.115-12C=
NM_001382763.1:c.115-12C=	NP_001369692.1:n.115-12C=
NM_001382764.1:c.115-12C=	NP_001369693.1:n.115-12C=
NM_001382765.1:c.115-12C=	NP_001369694.1:n.115-12C=
NM_005141.5:c.115-12C= MANE Select	NP_005132.2:n.115-12C=