Canonical Allele Identifier: CA1504935645

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569782C= , CM000666.2:g.154569782C=	GRCh38
NC_000004.11:g.155490934C= , CM000666.1:g.155490934C=	GRCh37
NC_000004.10:g.155710384C=	NCBI36
NG_008833.1:g.11803C= , LRG_558:g.11803C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1227C= MANE Select	ENSP00000306099.4:p.Asp409=
ENST00000302068.8:c.1227C=	ENSP00000306099.4:p.Asp409=
ENST00000502545.5:n.939+475C=
ENST00000509493.1:c.570C=	ENSP00000426757.1:p.Asp190=
NM_001184741.1:c.1050C=	NP_001171670.1:p.Asp350=
NM_005141.4:c.1227C= , LRG_558t1:c.1227C=	NP_005132.2:p.Asp409=
NM_001382759.1:c.1095C=	NP_001369688.1:p.Asp365=
NM_001382760.1:c.1227C=	NP_001369689.1:p.Asp409=
NM_001382761.1:c.1227C=	NP_001369690.1:p.Asp409=
NM_001382762.1:c.927C=	NP_001369691.1:p.Asp309=
NM_001382763.1:c.1218C=	NP_001369692.1:p.Asp406=
NM_001382764.1:c.*1C=	NP_001369693.1:n.*1C=
NM_001382765.1:c.1220+7C=	NP_001369694.1:n.1220+7C=
NM_005141.5:c.1227C= MANE Select	NP_005132.2:p.Asp409=