Canonical Allele Identifier: CA789366823

Gene: FGB

Linked Data

• dbSNP Id: rs1235001353
• MyVariant Identifiers: chr4:g.155486851_155486852insAATT (hg19) ; chr4:g.154565699_154565700insAATT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154565701_154565704dup , CM000666.2:g.154565701_154565704dup	GRCh38
NC_000004.11:g.155486853_155486856dup , CM000666.1:g.155486853_155486856dup	GRCh37
NC_000004.10:g.155706303_155706306dup	NCBI36
NG_008833.1:g.7722_7725dup , LRG_558:g.7722_7725dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.115-107_115-104dup MANE Select	ENSP00000306099.4:n.115-107_115-104dup
ENST00000302068.8:c.115-107_115-104dup	ENSP00000306099.4:n.115-107_115-104dup
ENST00000425838.5:c.*27-107_*27-104dup	ENSP00000398719.1:n.*27-107_*27-104dup
ENST00000497097.5:n.122-107_122-104dup
ENST00000498375.2:n.638_641dup
ENST00000502545.5:n.96-107_96-104dup
ENST00000509493.1:c.-167-1892_-167-1889dup	ENSP00000426757.1:n.-167-1892_-167-1889dup
NM_001184741.1:c.115-107_115-104dup	NP_001171670.1:n.115-107_115-104dup
NM_005141.4:c.115-107_115-104dup , LRG_558t1:c.115-107_115-104dup	NP_005132.2:n.115-107_115-104dup
NM_001382759.1:c.115-107_115-104dup	NP_001369688.1:n.115-107_115-104dup
NM_001382760.1:c.115-107_115-104dup	NP_001369689.1:n.115-107_115-104dup
NM_001382761.1:c.115-107_115-104dup	NP_001369690.1:n.115-107_115-104dup
NM_001382762.1:c.115-107_115-104dup	NP_001369691.1:n.115-107_115-104dup
NM_001382763.1:c.115-107_115-104dup	NP_001369692.1:n.115-107_115-104dup
NM_001382764.1:c.115-107_115-104dup	NP_001369693.1:n.115-107_115-104dup
NM_001382765.1:c.115-107_115-104dup	NP_001369694.1:n.115-107_115-104dup
NM_005141.5:c.115-107_115-104dup MANE Select	NP_005132.2:n.115-107_115-104dup