Canonical Allele Identifier: CA1504935224

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154565891C= , CM000666.2:g.154565891C=	GRCh38
NC_000004.11:g.155487043C= , CM000666.1:g.155487043C=	GRCh37
NC_000004.10:g.155706493C=	NCBI36
NG_008833.1:g.7912C= , LRG_558:g.7912C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.198C= MANE Select	ENSP00000306099.4:p.Ile66=
ENST00000302068.8:c.198C=	ENSP00000306099.4:p.Ile66=
ENST00000425838.5:c.*110C=	ENSP00000398719.1:n.*110C=
ENST00000473984.1:n.111C=
ENST00000497097.5:n.205C=
ENST00000498375.2:n.828C=
ENST00000502545.5:n.179C=
ENST00000509493.1:c.-167-1702C=	ENSP00000426757.1:n.-167-1702C=
NM_001184741.1:c.165+33C=	NP_001171670.1:n.165+33C=
NM_005141.4:c.198C= , LRG_558t1:c.198C=	NP_005132.2:p.Ile66=
NM_001382759.1:c.198C=	NP_001369688.1:p.Ile66=
NM_001382760.1:c.198C=	NP_001369689.1:p.Ile66=
NM_001382761.1:c.198C=	NP_001369690.1:p.Ile66=
NM_001382762.1:c.198C=	NP_001369691.1:p.Ile66=
NM_001382763.1:c.198C=	NP_001369692.1:p.Ile66=
NM_001382764.1:c.198C=	NP_001369693.1:p.Ile66=
NM_001382765.1:c.198C=	NP_001369694.1:p.Ile66=
NM_005141.5:c.198C= MANE Select	NP_005132.2:p.Ile66=