Canonical Allele Identifier: CA2695198550

Gene: FGB

Linked Data

• ClinVar Variation Id: 2637595
• ClinVar RCV Id: RCV003404893

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154566006_154566007delinsAA , CM000666.2:g.154566006_154566007delinsAA	GRCh38
NC_000004.11:g.155487158_155487159delinsAA , CM000666.1:g.155487158_155487159delinsAA	GRCh37
NC_000004.10:g.155706608_155706609delinsAA	NCBI36
NG_008833.1:g.8027_8028delinsAA , LRG_558:g.8027_8028delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.306+7_306+8delinsAA MANE Select	ENSP00000306099.4:n.306+7_306+8delinsAA
ENST00000302068.8:c.306+7_306+8delinsAA	ENSP00000306099.4:n.306+7_306+8delinsAA
ENST00000425838.5:c.*218+7_*218+8delinsAA	ENSP00000398719.1:n.*218+7_*218+8delinsAA
ENST00000473984.1:n.219+7_219+8delinsAA
ENST00000497097.5:n.313+7_313+8delinsAA
ENST00000498375.2:n.936+7_936+8delinsAA
ENST00000502545.5:n.287+7_287+8delinsAA
ENST00000509493.1:c.-167-1587_-167-1586delinsAA	ENSP00000426757.1:n.-167-1587_-167-1586delinsAA
NM_001184741.1:c.165+148_165+149delinsAA	NP_001171670.1:n.165+148_165+149delinsAA
NM_005141.4:c.306+7_306+8delinsAA , LRG_558t1:c.306+7_306+8delinsAA	NP_005132.2:n.306+7_306+8delinsAA
NM_001382759.1:c.306+7_306+8delinsAA	NP_001369688.1:n.306+7_306+8delinsAA
NM_001382760.1:c.306+7_306+8delinsAA	NP_001369689.1:n.306+7_306+8delinsAA
NM_001382761.1:c.306+7_306+8delinsAA	NP_001369690.1:n.306+7_306+8delinsAA
NM_001382762.1:c.306+7_306+8delinsAA	NP_001369691.1:n.306+7_306+8delinsAA
NM_001382763.1:c.306+7_306+8delinsAA	NP_001369692.1:n.306+7_306+8delinsAA
NM_001382764.1:c.306+7_306+8delinsAA	NP_001369693.1:n.306+7_306+8delinsAA
NM_001382765.1:c.306+7_306+8delinsAA	NP_001369694.1:n.306+7_306+8delinsAA
NM_005141.5:c.306+7_306+8delinsAA MANE Select	NP_005132.2:n.306+7_306+8delinsAA