Canonical Allele Identifier: CA645509078

Gene: SDHB

Linked Data

• ClinVar Variation Id: 438422
• ClinVar RCV Id: RCV000505290
• dbSNP Id: rs1553177687

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027842_17027844delinsAGATACC , CM000663.2:g.17027842_17027844delinsAGATACC	GRCh38
NC_000001.10:g.17354337_17354339delinsAGATACC , CM000663.1:g.17354337_17354339delinsAGATACC	GRCh37
NC_000001.9:g.17226924_17226926delinsAGATACC	NCBI36
NG_012340.1:g.31327_31329delinsGGTATCT , LRG_316:g.31327_31329delinsGGTATCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.274_276delinsGGTATCT	ENSP00000481376.2:p.Gln92GlyfsTer7
ENST00000491274.6:c.403_405delinsGGTATCT	ENSP00000480482.2:p.Gln135GlyfsTer7
ENST00000375499.8:c.445_447delinsGGTATCT MANE Select	ENSP00000364649.3:p.Gln149GlyfsTer7
ENST00000375499.7:c.445_447delinsGGTATCT	ENSP00000364649.3:p.Gln149GlyfsTer7
ENST00000463045.2:c.274_276delinsGGTATCT	ENSP00000481376.1:p.Gln92GlyfsTer7
ENST00000475506.1:n.362_364delinsGGTATCT
ENST00000485515.5:n.379_381delinsGGTATCT
ENST00000491274.5:c.403_405delinsGGTATCT	ENSP00000480482.1:p.Gln135GlyfsTer7
NM_003000.2:c.445_447delinsGGTATCT , LRG_316t1:c.445_447delinsGGTATCT	NP_002991.2:p.Gln149GlyfsTer7
NM_003000.3:c.445_447delinsGGTATCT MANE Select	NP_002991.2:p.Gln149GlyfsTer7