Canonical Allele Identifier: CA2740090529

Gene: SDHB

Linked Data

• ClinVar Variation Id: 2946972
• ClinVar RCV Id: RCV003801162

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027879_17027880insGAG , CM000663.2:g.17027879_17027880insGAG	GRCh38
NC_000001.10:g.17354374_17354375insGAG , CM000663.1:g.17354374_17354375insGAG	GRCh37
NC_000001.9:g.17226961_17226962insGAG	NCBI36
NG_012340.1:g.31292_31293insTCC , LRG_316:g.31292_31293insTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.253-14_253-13insTCC	ENSP00000481376.2:n.253-14_253-13insTCC
ENST00000491274.6:c.382-14_382-13insTCC	ENSP00000480482.2:n.382-14_382-13insTCC
ENST00000375499.8:c.424-14_424-13insTCC MANE Select	ENSP00000364649.3:n.424-14_424-13insTCC
ENST00000375499.7:c.424-14_424-13insTCC	ENSP00000364649.3:n.424-14_424-13insTCC
ENST00000463045.2:c.253-14_253-13insTCC	ENSP00000481376.1:n.253-14_253-13insTCC
ENST00000475506.1:n.341-14_341-13insTCC
ENST00000485515.5:n.358-14_358-13insTCC
ENST00000491274.5:c.382-14_382-13insTCC	ENSP00000480482.1:n.382-14_382-13insTCC
NM_003000.2:c.424-14_424-13insTCC , LRG_316t1:c.424-14_424-13insTCC	NP_002991.2:n.424-14_424-13insTCC
NM_003000.3:c.424-14_424-13insTCC MANE Select	NP_002991.2:n.424-14_424-13insTCC