Canonical Allele Identifier: CA1504935308

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569585A= , CM000666.2:g.154569585A=	GRCh38
NC_000004.11:g.155490737A= , CM000666.1:g.155490737A=	GRCh37
NC_000004.10:g.155710187A=	NCBI36
NG_008833.1:g.11606A= , LRG_558:g.11606A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1030A= MANE Select	ENSP00000306099.4:p.Met344=
ENST00000302068.8:c.1030A=	ENSP00000306099.4:p.Met344=
ENST00000502545.5:n.939+278A=
ENST00000509493.1:c.373A=	ENSP00000426757.1:p.Met125=
NM_001184741.1:c.853A=	NP_001171670.1:p.Met285=
NM_005141.4:c.1030A= , LRG_558t1:c.1030A=	NP_005132.2:p.Met344=
NM_001382759.1:c.898A=	NP_001369688.1:p.Met300=
NM_001382760.1:c.1030A=	NP_001369689.1:p.Met344=
NM_001382761.1:c.1030A=	NP_001369690.1:p.Met344=
NM_001382762.1:c.746-16A=	NP_001369691.1:n.746-16A=
NM_001382763.1:c.1021A=	NP_001369692.1:p.Met341=
NM_001382764.1:c.1030A=	NP_001369693.1:p.Met344=
NM_001382765.1:c.1030A=	NP_001369694.1:p.Met344=
NM_005141.5:c.1030A= MANE Select	NP_005132.2:p.Met344=