Canonical Allele Identifier: CA2740090607

Gene: SDHB

Linked Data

• ClinVar Variation Id: 2949579
• ClinVar RCV Id: RCV003804745

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044817del , CM000663.2:g.17044817del	GRCh38
NC_000001.10:g.17371312del , CM000663.1:g.17371312del	GRCh37
NC_000001.9:g.17243899del	NCBI36
NG_012340.1:g.14356del , LRG_316:g.14356del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-26del	ENSP00000481376.2:n.-26del
ENST00000491274.6:c.104del	ENSP00000480482.2:p.Pro35GlnfsTer28
ENST00000375499.8:c.146del MANE Select	ENSP00000364649.3:p.Pro49GlnfsTer28
ENST00000375499.7:c.146del	ENSP00000364649.3:p.Pro49GlnfsTer28
ENST00000463045.2:c.-26del	ENSP00000481376.1:n.-26del
ENST00000466613.2:n.158del
ENST00000475506.1:n.63del
ENST00000485515.5:n.134del
ENST00000491274.5:c.104del	ENSP00000480482.1:p.Pro35GlnfsTer28
NM_003000.2:c.146del , LRG_316t1:c.146del	NP_002991.2:p.Pro49GlnfsTer28
NM_003000.3:c.146del MANE Select	NP_002991.2:p.Pro49GlnfsTer28