Canonical Allele Identifier: CA1504935513

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569701C= , CM000666.2:g.154569701C=	GRCh38
NC_000004.11:g.155490853C= , CM000666.1:g.155490853C=	GRCh37
NC_000004.10:g.155710303C=	NCBI36
NG_008833.1:g.11722C= , LRG_558:g.11722C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1146C= MANE Select	ENSP00000306099.4:p.Ala382=
ENST00000302068.8:c.1146C=	ENSP00000306099.4:p.Ala382=
ENST00000502545.5:n.939+394C=
ENST00000509493.1:c.489C=	ENSP00000426757.1:p.Ala163=
NM_001184741.1:c.969C=	NP_001171670.1:p.Ala323=
NM_005141.4:c.1146C= , LRG_558t1:c.1146C=	NP_005132.2:p.Ala382=
NM_001382759.1:c.1014C=	NP_001369688.1:p.Ala338=
NM_001382760.1:c.1146C=	NP_001369689.1:p.Ala382=
NM_001382761.1:c.1146C=	NP_001369690.1:p.Ala382=
NM_001382762.1:c.846C=	NP_001369691.1:p.Ala282=
NM_001382763.1:c.1137C=	NP_001369692.1:p.Ala379=
NM_001382764.1:c.1080+66C=	NP_001369693.1:n.1080+66C=
NM_001382765.1:c.1146C=	NP_001369694.1:p.Ala382=
NM_005141.5:c.1146C= MANE Select	NP_005132.2:p.Ala382=