Canonical Allele Identifier: CA1156078037

Gene: SDHB

Linked Data

• ClinVar Variation Id: 2936823
• ClinVar RCV Id: RCV003799061
• dbSNP Id: rs2077969234

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022749_17022751dup , CM000663.2:g.17022749_17022751dup	GRCh38
NC_000001.10:g.17349244_17349246dup , CM000663.1:g.17349244_17349246dup	GRCh37
NC_000001.9:g.17221831_17221833dup	NCBI36
NG_012340.1:g.36421_36423dup , LRG_316:g.36421_36423dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.472-20_472-18dup	ENSP00000481376.2:n.472-20_472-18dup
ENST00000491274.6:c.601-20_601-18dup	ENSP00000480482.2:n.601-20_601-18dup
ENST00000375499.8:c.643-20_643-18dup MANE Select	ENSP00000364649.3:n.643-20_643-18dup
ENST00000375499.7:c.643-20_643-18dup	ENSP00000364649.3:n.643-20_643-18dup
ENST00000475049.5:n.68-20_68-18dup
ENST00000485092.5:n.287_289dup
ENST00000485515.5:n.577-20_577-18dup
NM_003000.2:c.643-20_643-18dup , LRG_316t1:c.643-20_643-18dup	NP_002991.2:n.643-20_643-18dup
NM_003000.3:c.643-20_643-18dup MANE Select	NP_002991.2:n.643-20_643-18dup