Canonical Allele Identifier: CA658798041

Gene: SDHB

Linked Data

• ClinVar Variation Id: 523118
• ClinVar RCV Id: RCV000626322

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17029671_17037575del , CM000663.2:g.17029671_17037575del	GRCh38
NC_000001.10:g.17356166_17364070del , CM000663.1:g.17356166_17364070del	GRCh37
NC_000001.9:g.17228753_17236657del	NCBI36
NG_012340.1:g.21597_29501del , LRG_316:g.21597_29501del

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.30-4429_116-934del
ENST00000491274.6:c.159-4429_245-934del
ENST00000375499.8:c.201-4429_287-934del
ENST00000375499.7:c.201-4429_287-934del
ENST00000463045.2:c.30-4429_116-934del
ENST00000475506.1:n.118-4429_204-934del
ENST00000485515.5:n.189-4429_275-934del
ENST00000491274.5:c.159-4429_245-934del
NM_003000.2:c.201-4429_287-934del , LRG_316t1:c.201-4429_287-934del
NM_003000.3:c.201-4429_287-934del