Canonical Allele Identifier: CA1504936038

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154570607G= , CM000666.2:g.154570607G=	GRCh38
NC_000004.11:g.155491759G= , CM000666.1:g.155491759G=	GRCh37
NC_000004.10:g.155711209G=	NCBI36
NG_008833.1:g.12628G= , LRG_558:g.12628G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1433G= MANE Select	ENSP00000306099.4:p.Arg478=
ENST00000302068.8:c.1433G=	ENSP00000306099.4:p.Arg478=
ENST00000502545.5:n.1128G=
ENST00000509493.1:c.776G=	ENSP00000426757.1:p.Arg259=
NM_001184741.1:c.1256G=	NP_001171670.1:p.Arg419=
NM_005141.4:c.1433G= , LRG_558t1:c.1433G=	NP_005132.2:p.Arg478=
NM_001382759.1:c.1301G=	NP_001369688.1:p.Arg434=
NM_001382760.1:c.1245-10G=	NP_001369689.1:n.1245-10G=
NM_001382761.1:c.*98G=	NP_001369690.1:n.*98G=
NM_001382762.1:c.1133G=	NP_001369691.1:p.Arg378=
NM_001382763.1:c.1424G=	NP_001369692.1:p.Arg475=
NM_001382764.1:c.*207G=	NP_001369693.1:n.*207G=
NM_001382765.1:c.1409G=	NP_001369694.1:p.Arg470=
NM_005141.5:c.1433G= MANE Select	NP_005132.2:p.Arg478=