Canonical Allele Identifier: CA416081919

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17349150_17349151insGCGGT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022655_17022656insGCGGT , CM000663.2:g.17022655_17022656insGCGGT	GRCh38
NC_000001.10:g.17349150_17349151insGCGGT , CM000663.1:g.17349150_17349151insGCGGT	GRCh37
NC_000001.9:g.17221737_17221738insGCGGT	NCBI36
NG_012340.1:g.36515_36516insACCGC , LRG_316:g.36515_36516insACCGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.546_547insACCGC	ENSP00000481376.2:p.Leu183ThrfsTer10
ENST00000491274.6:c.675_676insACCGC	ENSP00000480482.2:p.Leu226ThrfsTer10
ENST00000375499.8:c.717_718insACCGC MANE Select	ENSP00000364649.3:p.Leu240ThrfsTer10
ENST00000375499.7:c.717_718insACCGC	ENSP00000364649.3:p.Leu240ThrfsTer10
ENST00000475049.5:n.142_143insACCGC
ENST00000485092.5:n.381_382insACCGC
ENST00000485515.5:n.651_652insACCGC
NM_003000.2:c.717_718insACCGC , LRG_316t1:c.717_718insACCGC	NP_002991.2:p.Leu240ThrfsTer10
NM_003000.3:c.717_718insACCGC MANE Select	NP_002991.2:p.Leu240ThrfsTer10