Canonical Allele Identifier: CA2580611151

Gene: SDHB

Linked Data

• ClinVar Variation Id: 1371694
• ClinVar RCV Id: RCV001899634
• dbSNP Id: rs2101521836

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027845_17027846dup , CM000663.2:g.17027845_17027846dup	GRCh38
NC_000001.10:g.17354340_17354341dup , CM000663.1:g.17354340_17354341dup	GRCh37
NC_000001.9:g.17226927_17226928dup	NCBI36
NG_012340.1:g.31327_31328dup , LRG_316:g.31327_31328dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.274_275dup	ENSP00000481376.2:p.Gln92HisfsTer10
ENST00000491274.6:c.403_404dup	ENSP00000480482.2:p.Gln135HisfsTer10
ENST00000375499.8:c.445_446dup MANE Select	ENSP00000364649.3:p.Gln149HisfsTer10
ENST00000375499.7:c.445_446dup	ENSP00000364649.3:p.Gln149HisfsTer10
ENST00000463045.2:c.274_275dup	ENSP00000481376.1:p.Gln92HisfsTer10
ENST00000475506.1:n.362_363dup
ENST00000485515.5:n.379_380dup
ENST00000491274.5:c.403_404dup	ENSP00000480482.1:p.Gln135HisfsTer10
NM_003000.2:c.445_446dup , LRG_316t1:c.445_446dup	NP_002991.2:p.Gln149HisfsTer10
NM_003000.3:c.445_446dup MANE Select	NP_002991.2:p.Gln149HisfsTer10