Canonical Allele Identifier: CA1504935595

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569745T= , CM000666.2:g.154569745T=	GRCh38
NC_000004.11:g.155490897T= , CM000666.1:g.155490897T=	GRCh37
NC_000004.10:g.155710347T=	NCBI36
NG_008833.1:g.11766T= , LRG_558:g.11766T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1190T= MANE Select	ENSP00000306099.4:p.Met397=
ENST00000302068.8:c.1190T=	ENSP00000306099.4:p.Met397=
ENST00000502545.5:n.939+438T=
ENST00000509493.1:c.533T=	ENSP00000426757.1:p.Met178=
NM_001184741.1:c.1013T=	NP_001171670.1:p.Met338=
NM_005141.4:c.1190T= , LRG_558t1:c.1190T=	NP_005132.2:p.Met397=
NM_001382759.1:c.1058T=	NP_001369688.1:p.Met353=
NM_001382760.1:c.1190T=	NP_001369689.1:p.Met397=
NM_001382761.1:c.1190T=	NP_001369690.1:p.Met397=
NM_001382762.1:c.890T=	NP_001369691.1:p.Met297=
NM_001382763.1:c.1181T=	NP_001369692.1:p.Met394=
NM_001382764.1:c.1081-28T=	NP_001369693.1:n.1081-28T=
NM_001382765.1:c.1190T=	NP_001369694.1:p.Met397=
NM_005141.5:c.1190T= MANE Select	NP_005132.2:p.Met397=