Canonical Allele Identifier: CA1504935656

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569795G= , CM000666.2:g.154569795G=	GRCh38
NC_000004.11:g.155490947G= , CM000666.1:g.155490947G=	GRCh37
NC_000004.10:g.155710397G=	NCBI36
NG_008833.1:g.11816G= , LRG_558:g.11816G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1240G= MANE Select	ENSP00000306099.4:p.Gly414=
ENST00000302068.8:c.1240G=	ENSP00000306099.4:p.Gly414=
ENST00000502545.5:n.939+488G=
ENST00000509493.1:c.583G=	ENSP00000426757.1:p.Gly195=
NM_001184741.1:c.1063G=	NP_001171670.1:p.Gly355=
NM_005141.4:c.1240G= , LRG_558t1:c.1240G=	NP_005132.2:p.Gly414=
NM_001382759.1:c.1108G=	NP_001369688.1:p.Gly370=
NM_001382760.1:c.1240G=	NP_001369689.1:p.Gly414=
NM_001382761.1:c.1240G=	NP_001369690.1:p.Gly414=
NM_001382762.1:c.940G=	NP_001369691.1:p.Gly314=
NM_001382763.1:c.1231G=	NP_001369692.1:p.Gly411=
NM_001382764.1:c.*14G=	NP_001369693.1:n.*14G=
NM_001382765.1:c.1220+20G=	NP_001369694.1:n.1220+20G=
NM_005141.5:c.1240G= MANE Select	NP_005132.2:p.Gly414=