Canonical Allele Identifier: CA1504935790

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154570076T= , CM000666.2:g.154570076T=	GRCh38
NC_000004.11:g.155491228T= , CM000666.1:g.155491228T=	GRCh37
NC_000004.10:g.155710678T=	NCBI36
NG_008833.1:g.12097T= , LRG_558:g.12097T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1244+277T= MANE Select	ENSP00000306099.4:n.1244+277T=
ENST00000302068.8:c.1244+277T=	ENSP00000306099.4:n.1244+277T=
ENST00000502545.5:n.940-343T=
ENST00000509493.1:c.587+277T=	ENSP00000426757.1:n.587+277T=
NM_001184741.1:c.1067+277T=	NP_001171670.1:n.1067+277T=
NM_005141.4:c.1244+277T= , LRG_558t1:c.1244+277T=	NP_005132.2:n.1244+277T=
NM_001382759.1:c.1112+277T=	NP_001369688.1:n.1112+277T=
NM_001382760.1:c.1244+277T=	NP_001369689.1:n.1244+277T=
NM_001382761.1:c.1244+277T=	NP_001369690.1:n.1244+277T=
NM_001382762.1:c.944+277T=	NP_001369691.1:n.944+277T=
NM_001382763.1:c.1235+277T=	NP_001369692.1:n.1235+277T=
NM_001382764.1:c.*18+277T=	NP_001369693.1:n.*18+277T=
NM_001382765.1:c.1220+301T=	NP_001369694.1:n.1220+301T=
NM_005141.5:c.1244+277T= MANE Select	NP_005132.2:n.1244+277T=