Canonical Allele Identifier: CA1504935566

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569728G= , CM000666.2:g.154569728G=	GRCh38
NC_000004.11:g.155490880G= , CM000666.1:g.155490880G=	GRCh37
NC_000004.10:g.155710330G=	NCBI36
NG_008833.1:g.11749G= , LRG_558:g.11749G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1173G= MANE Select	ENSP00000306099.4:p.Met391=
ENST00000302068.8:c.1173G=	ENSP00000306099.4:p.Met391=
ENST00000502545.5:n.939+421G=
ENST00000509493.1:c.516G=	ENSP00000426757.1:p.Met172=
NM_001184741.1:c.996G=	NP_001171670.1:p.Met332=
NM_005141.4:c.1173G= , LRG_558t1:c.1173G=	NP_005132.2:p.Met391=
NM_001382759.1:c.1041G=	NP_001369688.1:p.Met347=
NM_001382760.1:c.1173G=	NP_001369689.1:p.Met391=
NM_001382761.1:c.1173G=	NP_001369690.1:p.Met391=
NM_001382762.1:c.873G=	NP_001369691.1:p.Met291=
NM_001382763.1:c.1164G=	NP_001369692.1:p.Met388=
NM_001382764.1:c.1081-45G=	NP_001369693.1:n.1081-45G=
NM_001382765.1:c.1173G=	NP_001369694.1:p.Met391=
NM_005141.5:c.1173G= MANE Select	NP_005132.2:p.Met391=