Canonical Allele Identifier: CA1504935402

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569648G= , CM000666.2:g.154569648G=	GRCh38
NC_000004.11:g.155490800G= , CM000666.1:g.155490800G=	GRCh37
NC_000004.10:g.155710250G=	NCBI36
NG_008833.1:g.11669G= , LRG_558:g.11669G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1093G= MANE Select	ENSP00000306099.4:p.Ala365=
ENST00000302068.8:c.1093G=	ENSP00000306099.4:p.Ala365=
ENST00000502545.5:n.939+341G=
ENST00000509493.1:c.436G=	ENSP00000426757.1:p.Ala146=
NM_001184741.1:c.916G=	NP_001171670.1:p.Ala306=
NM_005141.4:c.1093G= , LRG_558t1:c.1093G=	NP_005132.2:p.Ala365=
NM_001382759.1:c.961G=	NP_001369688.1:p.Ala321=
NM_001382760.1:c.1093G=	NP_001369689.1:p.Ala365=
NM_001382761.1:c.1093G=	NP_001369690.1:p.Ala365=
NM_001382762.1:c.793G=	NP_001369691.1:p.Ala265=
NM_001382763.1:c.1084G=	NP_001369692.1:p.Ala362=
NM_001382764.1:c.1080+13G=	NP_001369693.1:n.1080+13G=
NM_001382765.1:c.1093G=	NP_001369694.1:p.Ala365=
NM_005141.5:c.1093G= MANE Select	NP_005132.2:p.Ala365=