Canonical Allele Identifier: CA658655604

Gene: SDHB

Linked Data

• ClinVar Variation Id: 2497263
• ClinVar RCV Id: RCV003213718 ; RCV003779770

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044896T>C , CM000663.2:g.17044896T>C	GRCh38
NC_000001.10:g.17371391T>C , CM000663.1:g.17371391T>C	GRCh37
NC_000001.9:g.17243978T>C	NCBI36
NG_012340.1:g.14275A>G , LRG_316:g.14275A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-99-8A>G	ENSP00000481376.2:n.-99-8A>G
ENST00000491274.6:c.31-8A>G	ENSP00000480482.2:n.31-8A>G
ENST00000375499.8:c.73-8A>G MANE Select	ENSP00000364649.3:n.73-8A>G
ENST00000375499.7:c.73-8A>G	ENSP00000364649.3:n.73-8A>G
ENST00000463045.2:c.-99-8A>G	ENSP00000481376.1:n.-99-8A>G
ENST00000466613.2:n.85-8A>G
ENST00000485515.5:n.61-8A>G
ENST00000491274.5:c.31-8A>G	ENSP00000480482.1:n.31-8A>G
NM_003000.2:c.73-8A>G , LRG_316t1:c.73-8A>G	NP_002991.2:n.73-8A>G
NM_003000.3:c.73-8A>G MANE Select	NP_002991.2:n.73-8A>G