Canonical Allele Identifier: CA1156080473

Gene: SDHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028579_17028581delinsCAG , CM000663.2:g.17028579_17028581delinsCAG	GRCh38
NC_000001.10:g.17355074_17355076delinsCAG , CM000663.1:g.17355074_17355076delinsCAG	GRCh37
NC_000001.9:g.17227661_17227663delinsCAG	NCBI36
NG_012340.1:g.30590_30592delinsCTG , LRG_316:g.30590_30592delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.252+19_252+21delinsCTG	ENSP00000481376.2:n.252+19_252+21delinsCTG
ENST00000491274.6:c.381+19_381+21delinsCTG	ENSP00000480482.2:n.381+19_381+21delinsCTG
ENST00000375499.8:c.423+19_423+21delinsCTG MANE Select	ENSP00000364649.3:n.423+19_423+21delinsCTG
ENST00000375499.7:c.423+19_423+21delinsCTG	ENSP00000364649.3:n.423+19_423+21delinsCTG
ENST00000463045.2:c.252+19_252+21delinsCTG	ENSP00000481376.1:n.252+19_252+21delinsCTG
ENST00000475506.1:n.340+19_340+21delinsCTG
ENST00000485515.5:n.357+73_357+75delinsCTG
ENST00000491274.5:c.381+19_381+21delinsCTG	ENSP00000480482.1:n.381+19_381+21delinsCTG
NM_003000.2:c.423+19_423+21delinsCTG , LRG_316t1:c.423+19_423+21delinsCTG	NP_002991.2:n.423+19_423+21delinsCTG
NM_003000.3:c.423+19_423+21delinsCTG MANE Select	NP_002991.2:n.423+19_423+21delinsCTG