Canonical Allele Identifier: CA1504935649

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569784G= , CM000666.2:g.154569784G=	GRCh38
NC_000004.11:g.155490936G= , CM000666.1:g.155490936G=	GRCh37
NC_000004.10:g.155710386G=	NCBI36
NG_008833.1:g.11805G= , LRG_558:g.11805G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1229G= MANE Select	ENSP00000306099.4:p.Arg410=
ENST00000302068.8:c.1229G=	ENSP00000306099.4:p.Arg410=
ENST00000502545.5:n.939+477G=
ENST00000509493.1:c.572G=	ENSP00000426757.1:p.Arg191=
NM_001184741.1:c.1052G=	NP_001171670.1:p.Arg351=
NM_005141.4:c.1229G= , LRG_558t1:c.1229G=	NP_005132.2:p.Arg410=
NM_001382759.1:c.1097G=	NP_001369688.1:p.Arg366=
NM_001382760.1:c.1229G=	NP_001369689.1:p.Arg410=
NM_001382761.1:c.1229G=	NP_001369690.1:p.Arg410=
NM_001382762.1:c.929G=	NP_001369691.1:p.Arg310=
NM_001382763.1:c.1220G=	NP_001369692.1:p.Arg407=
NM_001382764.1:c.*3G=	NP_001369693.1:n.*3G=
NM_001382765.1:c.1220+9G=	NP_001369694.1:n.1220+9G=
NM_005141.5:c.1229G= MANE Select	NP_005132.2:p.Arg410=