Canonical Allele Identifier: CA2573130759

Gene: SDHB

Linked Data

• ClinVar Variation Id: 1456331
• ClinVar RCV Id: RCV001951091
• dbSNP Id: rs2101541632

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044887del , CM000663.2:g.17044887del	GRCh38
NC_000001.10:g.17371382del , CM000663.1:g.17371382del	GRCh37
NC_000001.9:g.17243969del	NCBI36
NG_012340.1:g.14285del , LRG_316:g.14285del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-97del	ENSP00000481376.2:n.-97del
ENST00000491274.6:c.33del	ENSP00000480482.2:p.Ser12ProfsTer?
ENST00000375499.8:c.75del MANE Select	ENSP00000364649.3:p.Ser26ProfsTer?
ENST00000375499.7:c.75del	ENSP00000364649.3:p.Ser26ProfsTer?
ENST00000463045.2:c.-97del	ENSP00000481376.1:n.-97del
ENST00000466613.2:n.87del
ENST00000485515.5:n.63del
ENST00000491274.5:c.33del	ENSP00000480482.1:p.Ser12ProfsTer?
NM_003000.2:c.75del , LRG_316t1:c.75del	NP_002991.2:p.Ser26ProfsTer?
NM_003000.3:c.75del MANE Select	NP_002991.2:p.Ser26ProfsTer?