Canonical Allele Identifier: CA1504935324

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569605C= , CM000666.2:g.154569605C=	GRCh38
NC_000004.11:g.155490757C= , CM000666.1:g.155490757C=	GRCh37
NC_000004.10:g.155710207C=	NCBI36
NG_008833.1:g.11626C= , LRG_558:g.11626C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1050C= MANE Select	ENSP00000306099.4:p.Asp350=
ENST00000302068.8:c.1050C=	ENSP00000306099.4:p.Asp350=
ENST00000502545.5:n.939+298C=
ENST00000509493.1:c.393C=	ENSP00000426757.1:p.Asp131=
NM_001184741.1:c.873C=	NP_001171670.1:p.Asp291=
NM_005141.4:c.1050C= , LRG_558t1:c.1050C=	NP_005132.2:p.Asp350=
NM_001382759.1:c.918C=	NP_001369688.1:p.Asp306=
NM_001382760.1:c.1050C=	NP_001369689.1:p.Asp350=
NM_001382761.1:c.1050C=	NP_001369690.1:p.Asp350=
NM_001382762.1:c.750C=	NP_001369691.1:p.Asp250=
NM_001382763.1:c.1041C=	NP_001369692.1:p.Asp347=
NM_001382764.1:c.1050C=	NP_001369693.1:p.Asp350=
NM_001382765.1:c.1050C=	NP_001369694.1:p.Asp350=
NM_005141.5:c.1050C= MANE Select	NP_005132.2:p.Asp350=