Canonical Allele Identifier: CA1504935658

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569799G= , CM000666.2:g.154569799G=	GRCh38
NC_000004.11:g.155490951G= , CM000666.1:g.155490951G=	GRCh37
NC_000004.10:g.155710401G=	NCBI36
NG_008833.1:g.11820G= , LRG_558:g.11820G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1244G= MANE Select	ENSP00000306099.4:p.Trp415=
ENST00000302068.8:c.1244G=	ENSP00000306099.4:p.Trp415=
ENST00000502545.5:n.939+492G=
ENST00000509493.1:c.587G=	ENSP00000426757.1:p.Trp196=
NM_001184741.1:c.1067G=	NP_001171670.1:p.Trp356=
NM_005141.4:c.1244G= , LRG_558t1:c.1244G=	NP_005132.2:p.Trp415=
NM_001382759.1:c.1112G=	NP_001369688.1:p.Trp371=
NM_001382760.1:c.1244G=	NP_001369689.1:p.Cys415=
NM_001382761.1:c.1244G=	NP_001369690.1:p.Ter415=
NM_001382762.1:c.944G=	NP_001369691.1:p.Trp315=
NM_001382763.1:c.1235G=	NP_001369692.1:p.Trp412=
NM_001382764.1:c.*18G=	NP_001369693.1:n.*18G=
NM_001382765.1:c.1220+24G=	NP_001369694.1:n.1220+24G=
NM_005141.5:c.1244G= MANE Select	NP_005132.2:p.Trp415=