Canonical Allele Identifier: CA279930

Gene: SDHB

Linked Data

• ClinVar Variation Id: 219155
• ClinVar RCV Id: RCV000203529
• dbSNP Id: rs864321639
• MyVariant Identifiers: chr1:g.17371317_17371325del (hg19) ; chr1:g.17044822_17044830del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044822_17044830del , CM000663.2:g.17044822_17044830del	GRCh38
NC_000001.10:g.17371317_17371325del , CM000663.1:g.17371317_17371325del	GRCh37
NC_000001.9:g.17243904_17243912del	NCBI36
NG_012340.1:g.14341_14349del , LRG_316:g.14341_14349del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-41_-33del	ENSP00000481376.2:n.-41_-33del
ENST00000491274.6:c.89_97del	ENSP00000480482.2:p.Ile30_Trp33delinsArg
ENST00000375499.8:c.131_139del MANE Select	ENSP00000364649.3:p.Ile44_Trp47delinsArg
ENST00000375499.7:c.131_139del	ENSP00000364649.3:p.Ile44_Trp47delinsArg
ENST00000463045.2:c.-41_-33del	ENSP00000481376.1:n.-41_-33del
ENST00000466613.2:n.143_151del
ENST00000475506.1:n.48_56del
ENST00000485515.5:n.119_127del
ENST00000491274.5:c.89_97del	ENSP00000480482.1:p.Ile30_Trp33delinsArg
NM_003000.2:c.131_139del , LRG_316t1:c.131_139del	NP_002991.2:p.Ile44_Trp47delinsArg
NM_003000.3:c.131_139del MANE Select	NP_002991.2:p.Ile44_Trp47delinsArg