Canonical Allele Identifier: CA358513134

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569202C>T , CM000666.2:g.154569202C>T	GRCh38
NC_000004.11:g.155490354C>T , CM000666.1:g.155490354C>T	GRCh37
NC_000004.10:g.155709804C>T	NCBI36
NG_008833.1:g.11223C>T , LRG_558:g.11223C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005141.5:c.853C>T MANE Select	NP_005132.2:p.Arg285Cys
ENST00000302068.9:c.853C>T MANE Select	ENSP00000306099.4:p.Arg285Cys
NM_001184741.1:c.676C>T	NP_001171670.1:p.Arg226Cys
NM_001382759.1:c.721C>T	NP_001369688.1:p.Arg241Cys
NM_001382760.1:c.853C>T	NP_001369689.1:p.Arg285Cys
NM_001382761.1:c.853C>T	NP_001369690.1:p.Arg285Cys
NM_001382762.1:c.746-399C>T	NP_001369691.1:n.746-399C>T
NM_001382763.1:c.844C>T	NP_001369692.1:p.Arg282Cys
NM_001382764.1:c.853C>T	NP_001369693.1:p.Arg285Cys
NM_001382765.1:c.853C>T	NP_001369694.1:p.Arg285Cys
NM_005141.4:c.853C>T , LRG_558t1:c.853C>T	NP_005132.2:p.Arg285Cys
ENST00000302068.8:c.853C>T	ENSP00000306099.4:p.Arg285Cys
ENST00000502545.5:n.834C>T
ENST00000509493.1:c.196C>T	ENSP00000426757.1:p.Arg66Cys