Canonical Allele Identifier: CA1504935776

Gene: FGB

Linked Data

• dbSNP Id: rs1730353713

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154570043dup , CM000666.2:g.154570043dup	GRCh38
NC_000004.11:g.155491195dup , CM000666.1:g.155491195dup	GRCh37
NC_000004.10:g.155710645dup	NCBI36
NG_008833.1:g.12064dup , LRG_558:g.12064dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1244+244dup MANE Select	ENSP00000306099.4:n.1244+244dup
ENST00000302068.8:c.1244+244dup	ENSP00000306099.4:n.1244+244dup
ENST00000502545.5:n.940-376dup
ENST00000509493.1:c.587+244dup	ENSP00000426757.1:n.587+244dup
NM_001184741.1:c.1067+244dup	NP_001171670.1:n.1067+244dup
NM_005141.4:c.1244+244dup , LRG_558t1:c.1244+244dup	NP_005132.2:n.1244+244dup
NM_001382759.1:c.1112+244dup	NP_001369688.1:n.1112+244dup
NM_001382760.1:c.1244+244dup	NP_001369689.1:n.1244+244dup
NM_001382761.1:c.1244+244dup	NP_001369690.1:n.1244+244dup
NM_001382762.1:c.944+244dup	NP_001369691.1:n.944+244dup
NM_001382763.1:c.1235+244dup	NP_001369692.1:n.1235+244dup
NM_001382764.1:c.*18+244dup	NP_001369693.1:n.*18+244dup
NM_001382765.1:c.1220+268dup	NP_001369694.1:n.1220+268dup
NM_005141.5:c.1244+244dup MANE Select	NP_005132.2:n.1244+244dup