Canonical Allele Identifier: CA1504934050

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154568456C= , CM000666.2:g.154568456C=	GRCh38
NC_000004.11:g.155489608C= , CM000666.1:g.155489608C=	GRCh37
NC_000004.10:g.155709058C=	NCBI36
NG_008833.1:g.10477C= , LRG_558:g.10477C=

Transcript Alleles

HGVS	Amino-acid Change
NM_005141.5:c.794C= MANE Select	NP_005132.2:p.Pro265=
ENST00000302068.9:c.794C= MANE Select	ENSP00000306099.4:p.Pro265=
NM_001184741.1:c.617C=	NP_001171670.1:p.Pro206=
NM_001382759.1:c.662C=	NP_001369688.1:p.Pro221=
NM_001382760.1:c.794C=	NP_001369689.1:p.Pro265=
NM_001382761.1:c.794C=	NP_001369690.1:p.Pro265=
NM_001382762.1:c.745+49C=	NP_001369691.1:n.745+49C=
NM_001382763.1:c.794C=	NP_001369692.1:p.Pro265=
NM_001382764.1:c.794C=	NP_001369693.1:p.Pro265=
NM_001382765.1:c.794C=	NP_001369694.1:p.Pro265=
NM_005141.4:c.794C= , LRG_558t1:c.794C=	NP_005132.2:p.Pro265=
ENST00000302068.8:c.794C=	ENSP00000306099.4:p.Pro265=
ENST00000502545.5:n.775C=
ENST00000509493.1:c.137C=	ENSP00000426757.1:p.Pro46=