Canonical Allele Identifier: CA1504935147

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154565833G= , CM000666.2:g.154565833G=	GRCh38
NC_000004.11:g.155486985G= , CM000666.1:g.155486985G=	GRCh37
NC_000004.10:g.155706435G=	NCBI36
NG_008833.1:g.7854G= , LRG_558:g.7854G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.140G= MANE Select	ENSP00000306099.4:p.Arg47=
ENST00000302068.8:c.140G=	ENSP00000306099.4:p.Arg47=
ENST00000425838.5:c.*52G=	ENSP00000398719.1:n.*52G=
ENST00000473984.1:n.53G=
ENST00000497097.5:n.147G=
ENST00000498375.2:n.770G=
ENST00000502545.5:n.121G=
ENST00000509493.1:c.-167-1760G=	ENSP00000426757.1:n.-167-1760G=
NM_001184741.1:c.140G=	NP_001171670.1:p.Arg47=
NM_005141.4:c.140G= , LRG_558t1:c.140G=	NP_005132.2:p.Arg47=
NM_001382759.1:c.140G=	NP_001369688.1:p.Arg47=
NM_001382760.1:c.140G=	NP_001369689.1:p.Arg47=
NM_001382761.1:c.140G=	NP_001369690.1:p.Arg47=
NM_001382762.1:c.140G=	NP_001369691.1:p.Arg47=
NM_001382763.1:c.140G=	NP_001369692.1:p.Arg47=
NM_001382764.1:c.140G=	NP_001369693.1:p.Arg47=
NM_001382765.1:c.140G=	NP_001369694.1:p.Arg47=
NM_005141.5:c.140G= MANE Select	NP_005132.2:p.Arg47=