Canonical Allele Identifier: CA1504935328

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154566001T= , CM000666.2:g.154566001T=	GRCh38
NC_000004.11:g.155487153T= , CM000666.1:g.155487153T=	GRCh37
NC_000004.10:g.155706603T=	NCBI36
NG_008833.1:g.8022T= , LRG_558:g.8022T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.306+2T= MANE Select	ENSP00000306099.4:n.306+2T=
ENST00000302068.8:c.306+2T=	ENSP00000306099.4:n.306+2T=
ENST00000425838.5:c.*218+2T=	ENSP00000398719.1:n.*218+2T=
ENST00000473984.1:n.219+2T=
ENST00000497097.5:n.313+2T=
ENST00000498375.2:n.936+2T=
ENST00000502545.5:n.287+2T=
ENST00000509493.1:c.-167-1592T=	ENSP00000426757.1:n.-167-1592T=
NM_001184741.1:c.165+143T=	NP_001171670.1:n.165+143T=
NM_005141.4:c.306+2T= , LRG_558t1:c.306+2T=	NP_005132.2:n.306+2T=
NM_001382759.1:c.306+2T=	NP_001369688.1:n.306+2T=
NM_001382760.1:c.306+2T=	NP_001369689.1:n.306+2T=
NM_001382761.1:c.306+2T=	NP_001369690.1:n.306+2T=
NM_001382762.1:c.306+2T=	NP_001369691.1:n.306+2T=
NM_001382763.1:c.306+2T=	NP_001369692.1:n.306+2T=
NM_001382764.1:c.306+2T=	NP_001369693.1:n.306+2T=
NM_001382765.1:c.306+2T=	NP_001369694.1:n.306+2T=
NM_005141.5:c.306+2T= MANE Select	NP_005132.2:n.306+2T=