Canonical Allele Identifier: CA1504935153

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154565835C= , CM000666.2:g.154565835C=	GRCh38
NC_000004.11:g.155486987C= , CM000666.1:g.155486987C=	GRCh37
NC_000004.10:g.155706437C=	NCBI36
NG_008833.1:g.7856C= , LRG_558:g.7856C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.142C= MANE Select	ENSP00000306099.4:p.Pro48=
ENST00000302068.8:c.142C=	ENSP00000306099.4:p.Pro48=
ENST00000425838.5:c.*54C=	ENSP00000398719.1:n.*54C=
ENST00000473984.1:n.55C=
ENST00000497097.5:n.149C=
ENST00000498375.2:n.772C=
ENST00000502545.5:n.123C=
ENST00000509493.1:c.-167-1758C=	ENSP00000426757.1:n.-167-1758C=
NM_001184741.1:c.142C=	NP_001171670.1:p.Pro48=
NM_005141.4:c.142C= , LRG_558t1:c.142C=	NP_005132.2:p.Pro48=
NM_001382759.1:c.142C=	NP_001369688.1:p.Pro48=
NM_001382760.1:c.142C=	NP_001369689.1:p.Pro48=
NM_001382761.1:c.142C=	NP_001369690.1:p.Pro48=
NM_001382762.1:c.142C=	NP_001369691.1:p.Pro48=
NM_001382763.1:c.142C=	NP_001369692.1:p.Pro48=
NM_001382764.1:c.142C=	NP_001369693.1:p.Pro48=
NM_001382765.1:c.142C=	NP_001369694.1:p.Pro48=
NM_005141.5:c.142C= MANE Select	NP_005132.2:p.Pro48=