Canonical Allele Identifier: CA1156077959

Gene: SDHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022593_17022597delinsACCAG , CM000663.2:g.17022593_17022597delinsACCAG	GRCh38
NC_000001.10:g.17349088_17349092delinsACCAG , CM000663.1:g.17349088_17349092delinsACCAG	GRCh37
NC_000001.9:g.17221675_17221679delinsACCAG	NCBI36
NG_012340.1:g.36574_36578delinsCTGGT , LRG_316:g.36574_36578delinsCTGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.594+11_594+15delinsCTGGT	ENSP00000481376.2:n.594+11_594+15delinsCTGGT
ENST00000491274.6:c.723+11_723+15delinsCTGGT	ENSP00000480482.2:n.723+11_723+15delinsCTGGT
ENST00000375499.8:c.765+11_765+15delinsCTGGT MANE Select	ENSP00000364649.3:n.765+11_765+15delinsCTGGT
ENST00000375499.7:c.765+11_765+15delinsCTGGT	ENSP00000364649.3:n.765+11_765+15delinsCTGGT
ENST00000475049.5:n.190+11_190+15delinsCTGGT
ENST00000485092.5:n.429+11_429+15delinsCTGGT
NM_003000.2:c.765+11_765+15delinsCTGGT , LRG_316t1:c.765+11_765+15delinsCTGGT	NP_002991.2:n.765+11_765+15delinsCTGGT
NM_003000.3:c.765+11_765+15delinsCTGGT MANE Select	NP_002991.2:n.765+11_765+15delinsCTGGT