Canonical Allele Identifier: CA2740090605

Gene: SDHB

Linked Data

• ClinVar Variation Id: 2936794
• ClinVar RCV Id: RCV003799032

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028754_17028756del , CM000663.2:g.17028754_17028756del	GRCh38
NC_000001.10:g.17355249_17355251del , CM000663.1:g.17355249_17355251del	GRCh37
NC_000001.9:g.17227836_17227838del	NCBI36
NG_012340.1:g.30415_30417del , LRG_316:g.30415_30417del

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.116-20_116-18del	ENSP00000481376.2:n.116-20_116-18del
ENST00000491274.6:c.245-20_245-18del	ENSP00000480482.2:n.245-20_245-18del
ENST00000375499.8:c.287-20_287-18del MANE Select	ENSP00000364649.3:n.287-20_287-18del
ENST00000375499.7:c.287-20_287-18del	ENSP00000364649.3:n.287-20_287-18del
ENST00000463045.2:c.116-20_116-18del	ENSP00000481376.1:n.116-20_116-18del
ENST00000475506.1:n.204-20_204-18del
ENST00000485515.5:n.275-20_275-18del
ENST00000491274.5:c.245-20_245-18del	ENSP00000480482.1:n.245-20_245-18del
NM_003000.2:c.287-20_287-18del , LRG_316t1:c.287-20_287-18del	NP_002991.2:n.287-20_287-18del
NM_003000.3:c.287-20_287-18del MANE Select	NP_002991.2:n.287-20_287-18del