Canonical Allele Identifier: CA2838032012
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027844_17027845delinsCCATAGA , CM000663.2:g.17027844_17027845delinsCCATAGA GRCh38
NC_000001.10:g.17354339_17354340delinsCCATAGA , CM000663.1:g.17354339_17354340delinsCCATAGA GRCh37
NC_000001.9:g.17226926_17226927delinsCCATAGA NCBI36
NG_012340.1:g.31326_31327delinsTCTATGG , LRG_316:g.31326_31327delinsTCTATGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.273_274delinsTCTATGG ENSP00000481376.2:p.Gln92LeufsTer11
ENST00000491274.6:c.402_403delinsTCTATGG ENSP00000480482.2:p.Gln135LeufsTer11
ENST00000375499.8:c.444_445delinsTCTATGG MANE Select ENSP00000364649.3:p.Gln149LeufsTer11
ENST00000375499.7:c.444_445delinsTCTATGG ENSP00000364649.3:p.Gln149LeufsTer11
ENST00000463045.2:c.273_274delinsTCTATGG ENSP00000481376.1:p.Gln92LeufsTer11
ENST00000475506.1:n.361_362delinsTCTATGG
ENST00000485515.5:n.378_379delinsTCTATGG
ENST00000491274.5:c.402_403delinsTCTATGG ENSP00000480482.1:p.Gln135LeufsTer11
NM_003000.2:c.444_445delinsTCTATGG , LRG_316t1:c.444_445delinsTCTATGG NP_002991.2:p.Gln149LeufsTer11
NM_003000.3:c.444_445delinsTCTATGG MANE Select NP_002991.2:p.Gln149LeufsTer11