Canonical Allele Identifier: CA891862655

Gene: SDHB

Linked Data

• ClinVar Variation Id: 591278
• ClinVar RCV Id: RCV000722456
• dbSNP Id: rs1557746639

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044826_17044827insGTTTCAACTTGTA , CM000663.2:g.17044826_17044827insGTTTCAACTTGTA	GRCh38
NC_000001.10:g.17371321_17371322insGTTTCAACTTGTA , CM000663.1:g.17371321_17371322insGTTTCAACTTGTA	GRCh37
NC_000001.9:g.17243908_17243909insGTTTCAACTTGTA	NCBI36
NG_012340.1:g.14345_14346insACAAGTTGAAACT , LRG_316:g.14345_14346insACAAGTTGAAACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-37_-36insACAAGTTGAAACT	ENSP00000481376.2:n.-37_-36insACAAGTTGAAACT
ENST00000491274.6:c.93_94insACAAGTTGAAACT	ENSP00000480482.2:p.Arg32ThrfsTer3
ENST00000375499.8:c.135_136insACAAGTTGAAACT MANE Select	ENSP00000364649.3:p.Arg46ThrfsTer3
ENST00000375499.7:c.135_136insACAAGTTGAAACT	ENSP00000364649.3:p.Arg46ThrfsTer3
ENST00000463045.2:c.-37_-36insACAAGTTGAAACT	ENSP00000481376.1:n.-37_-36insACAAGTTGAAACT
ENST00000466613.2:n.147_148insACAAGTTGAAACT
ENST00000475506.1:n.52_53insACAAGTTGAAACT
ENST00000485515.5:n.123_124insACAAGTTGAAACT
ENST00000491274.5:c.93_94insACAAGTTGAAACT	ENSP00000480482.1:p.Arg32ThrfsTer3
NM_003000.2:c.135_136insACAAGTTGAAACT , LRG_316t1:c.135_136insACAAGTTGAAACT	NP_002991.2:p.Arg46ThrfsTer3
NM_003000.3:c.135_136insACAAGTTGAAACT MANE Select	NP_002991.2:p.Arg46ThrfsTer3