Canonical Allele Identifier: CA2586964056

Gene: SDHB

Linked Data

• ClinVar Variation Id: 2943394
• ClinVar RCV Id: RCV003800512

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027781dup , CM000663.2:g.17027781dup	GRCh38
NC_000001.10:g.17354276dup , CM000663.1:g.17354276dup	GRCh37
NC_000001.9:g.17226863dup	NCBI36
NG_012340.1:g.31390dup , LRG_316:g.31390dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.337dup	ENSP00000481376.2:p.Tyr113LeufsTer9
ENST00000491274.6:c.466dup	ENSP00000480482.2:p.Tyr156LeufsTer9
ENST00000375499.8:c.508dup MANE Select	ENSP00000364649.3:p.Tyr170LeufsTer9
ENST00000375499.7:c.508dup	ENSP00000364649.3:p.Tyr170LeufsTer9
ENST00000463045.2:c.337dup	ENSP00000481376.1:p.Tyr113LeufsTer9
ENST00000475506.1:n.425dup
ENST00000485515.5:n.442dup
ENST00000491274.5:c.466dup	ENSP00000480482.1:p.Tyr156LeufsTer9
NM_003000.2:c.508dup , LRG_316t1:c.508dup	NP_002991.2:p.Tyr170LeufsTer9
NM_003000.3:c.508dup MANE Select	NP_002991.2:p.Tyr170LeufsTer9