Canonical Allele Identifier: CA1504935660

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569801T= , CM000666.2:g.154569801T=	GRCh38
NC_000004.11:g.155490953T= , CM000666.1:g.155490953T=	GRCh37
NC_000004.10:g.155710403T=	NCBI36
NG_008833.1:g.11822T= , LRG_558:g.11822T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1244+2T= MANE Select	ENSP00000306099.4:n.1244+2T=
ENST00000302068.8:c.1244+2T=	ENSP00000306099.4:n.1244+2T=
ENST00000502545.5:n.939+494T=
ENST00000509493.1:c.587+2T=	ENSP00000426757.1:n.587+2T=
NM_001184741.1:c.1067+2T=	NP_001171670.1:n.1067+2T=
NM_005141.4:c.1244+2T= , LRG_558t1:c.1244+2T=	NP_005132.2:n.1244+2T=
NM_001382759.1:c.1112+2T=	NP_001369688.1:n.1112+2T=
NM_001382760.1:c.1244+2T=	NP_001369689.1:n.1244+2T=
NM_001382761.1:c.1244+2T=	NP_001369690.1:n.1244+2T=
NM_001382762.1:c.944+2T=	NP_001369691.1:n.944+2T=
NM_001382763.1:c.1235+2T=	NP_001369692.1:n.1235+2T=
NM_001382764.1:c.*18+2T=	NP_001369693.1:n.*18+2T=
NM_001382765.1:c.1220+26T=	NP_001369694.1:n.1220+26T=
NM_005141.5:c.1244+2T= MANE Select	NP_005132.2:n.1244+2T=