Canonical Allele Identifier: CA2586964062

Gene: SDHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027843_17027844delinsAGATACC , CM000663.2:g.17027843_17027844delinsAGATACC	GRCh38
NC_000001.10:g.17354338_17354339delinsAGATACC , CM000663.1:g.17354338_17354339delinsAGATACC	GRCh37
NC_000001.9:g.17226925_17226926delinsAGATACC	NCBI36
NG_012340.1:g.31327_31328delinsGGTATCT , LRG_316:g.31327_31328delinsGGTATCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.274_275delinsGGTATCT	ENSP00000481376.2:p.Gln92GlyfsTer11
ENST00000491274.6:c.403_404delinsGGTATCT	ENSP00000480482.2:p.Gln135GlyfsTer11
ENST00000375499.8:c.445_446delinsGGTATCT MANE Select	ENSP00000364649.3:p.Gln149GlyfsTer11
ENST00000375499.7:c.445_446delinsGGTATCT	ENSP00000364649.3:p.Gln149GlyfsTer11
ENST00000463045.2:c.274_275delinsGGTATCT	ENSP00000481376.1:p.Gln92GlyfsTer11
ENST00000475506.1:n.362_363delinsGGTATCT
ENST00000485515.5:n.379_380delinsGGTATCT
ENST00000491274.5:c.403_404delinsGGTATCT	ENSP00000480482.1:p.Gln135GlyfsTer11
NM_003000.2:c.445_446delinsGGTATCT , LRG_316t1:c.445_446delinsGGTATCT	NP_002991.2:p.Gln149GlyfsTer11
NM_003000.3:c.445_446delinsGGTATCT MANE Select	NP_002991.2:p.Gln149GlyfsTer11