Canonical Allele Identifier: CA1139655462

Gene: SDHB

Linked Data

• ClinVar Variation Id: 944109
• ClinVar RCV Id: RCV001214438
• dbSNP Id: rs2077969156

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022733_17022738del , CM000663.2:g.17022733_17022738del	GRCh38
NC_000001.10:g.17349228_17349233del , CM000663.1:g.17349228_17349233del	GRCh37
NC_000001.9:g.17221815_17221820del	NCBI36
NG_012340.1:g.36433_36438del , LRG_316:g.36433_36438del

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.472-8_472-3del	ENSP00000481376.2:n.472-8_472-3del
ENST00000491274.6:c.601-8_601-3del	ENSP00000480482.2:n.601-8_601-3del
ENST00000375499.8:c.643-8_643-3del MANE Select	ENSP00000364649.3:n.643-8_643-3del
ENST00000375499.7:c.643-8_643-3del	ENSP00000364649.3:n.643-8_643-3del
ENST00000475049.5:n.68-8_68-3del
ENST00000485092.5:n.299_304del
ENST00000485515.5:n.577-8_577-3del
NM_003000.2:c.643-8_643-3del , LRG_316t1:c.643-8_643-3del	NP_002991.2:n.643-8_643-3del
NM_003000.3:c.643-8_643-3del MANE Select	NP_002991.2:n.643-8_643-3del