Canonical Allele Identifier: CA2741808821

Gene: FGB

Linked Data

• ClinVar Variation Id: 16381
• ClinVar RCV Id: RCV000017803

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154565809_154566000del , CM000666.2:g.154565809_154566000del	GRCh38
NC_000004.11:g.155486961_155487152del , CM000666.1:g.155486961_155487152del	GRCh37
NC_000004.10:g.155706411_155706602del	NCBI36
NG_008833.1:g.7830_8021del , LRG_558:g.7830_8021del

Transcript Alleles

HGVS	Amino-acid change
ENST00000302068.9:c.116_306+1del
ENST00000302068.8:c.116_306+1del
ENST00000425838.5:c.*28_*218+1del
ENST00000473984.1:n.29_219+1del
ENST00000497097.5:n.123_313+1del
ENST00000498375.2:n.746_936+1del
ENST00000502545.5:n.97_287+1del
ENST00000509493.1:c.-167-1784_-167-1593del	ENSP00000426757.1:n.-167-1784_-167-1593del
NM_001184741.1:c.116_165+142del
NM_005141.4:c.116_306+1del , LRG_558t1:c.116_306+1del
NM_001382759.1:c.116_306+1del
NM_001382760.1:c.116_306+1del
NM_001382761.1:c.116_306+1del
NM_001382762.1:c.116_306+1del
NM_001382763.1:c.116_306+1del
NM_001382764.1:c.116_306+1del
NM_001382765.1:c.116_306+1del
NM_005141.5:c.116_306+1del