Canonical Allele Identifier: CA108749221

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154563359G>A , CM000666.2:g.154563359G>A	GRCh38
NC_000004.11:g.155484511G>A , CM000666.1:g.155484511G>A	GRCh37
NC_000004.10:g.155703961G>A	NCBI36
NG_008833.1:g.5380G>A , LRG_558:g.5380G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005141.5:c.114+227G>A MANE Select	NP_005132.2:n.114+227G>A
ENST00000302068.9:c.114+227G>A MANE Select	ENSP00000306099.4:n.114+227G>A
NM_001184741.1:c.114+227G>A	NP_001171670.1:n.114+227G>A
NM_001382759.1:c.114+227G>A	NP_001369688.1:n.114+227G>A
NM_001382760.1:c.114+227G>A	NP_001369689.1:n.114+227G>A
NM_001382761.1:c.114+227G>A	NP_001369690.1:n.114+227G>A
NM_001382762.1:c.114+227G>A	NP_001369691.1:n.114+227G>A
NM_001382763.1:c.114+227G>A	NP_001369692.1:n.114+227G>A
NM_001382764.1:c.114+227G>A	NP_001369693.1:n.114+227G>A
NM_001382765.1:c.114+227G>A	NP_001369694.1:n.114+227G>A
NM_005141.4:c.114+227G>A , LRG_558t1:c.114+227G>A	NP_005132.2:n.114+227G>A
ENST00000302068.8:c.114+227G>A	ENSP00000306099.4:n.114+227G>A
ENST00000425838.5:c.114+227G>A	ENSP00000398719.1:n.114+227G>A
ENST00000497097.5:n.121+227G>A
ENST00000498375.2:n.122+227G>A
ENST00000502545.5:n.95+227G>A
ENST00000509493.1:c.-168+227G>A	ENSP00000426757.1:n.-168+227G>A