Canonical Allele Identifier: CA1504935590

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569743C= , CM000666.2:g.154569743C=	GRCh38
NC_000004.11:g.155490895C= , CM000666.1:g.155490895C=	GRCh37
NC_000004.10:g.155710345C=	NCBI36
NG_008833.1:g.11764C= , LRG_558:g.11764C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1188C= MANE Select	ENSP00000306099.4:p.Thr396=
ENST00000302068.8:c.1188C=	ENSP00000306099.4:p.Thr396=
ENST00000502545.5:n.939+436C=
ENST00000509493.1:c.531C=	ENSP00000426757.1:p.Thr177=
NM_001184741.1:c.1011C=	NP_001171670.1:p.Thr337=
NM_005141.4:c.1188C= , LRG_558t1:c.1188C=	NP_005132.2:p.Thr396=
NM_001382759.1:c.1056C=	NP_001369688.1:p.Thr352=
NM_001382760.1:c.1188C=	NP_001369689.1:p.Thr396=
NM_001382761.1:c.1188C=	NP_001369690.1:p.Thr396=
NM_001382762.1:c.888C=	NP_001369691.1:p.Thr296=
NM_001382763.1:c.1179C=	NP_001369692.1:p.Thr393=
NM_001382764.1:c.1081-30C=	NP_001369693.1:n.1081-30C=
NM_001382765.1:c.1188C=	NP_001369694.1:p.Thr396=
NM_005141.5:c.1188C= MANE Select	NP_005132.2:p.Thr396=