Canonical Allele Identifier: CA916081283

Gene: SDHB

Linked Data

• ClinVar Variation Id: 837850
• ClinVar RCV Id: RCV001039278
• dbSNP Id: rs2077967877

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022605T>A , CM000663.2:g.17022605T>A	GRCh38
NC_000001.10:g.17349100T>A , CM000663.1:g.17349100T>A	GRCh37
NC_000001.9:g.17221687T>A	NCBI36
NG_012340.1:g.36566A>T , LRG_316:g.36566A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.594+3A>T	ENSP00000481376.2:n.594+3A>T
ENST00000491274.6:c.723+3A>T	ENSP00000480482.2:n.723+3A>T
ENST00000375499.8:c.765+3A>T MANE Select	ENSP00000364649.3:n.765+3A>T
ENST00000375499.7:c.765+3A>T	ENSP00000364649.3:n.765+3A>T
ENST00000475049.5:n.190+3A>T
ENST00000485092.5:n.429+3A>T
NM_003000.2:c.765+3A>T , LRG_316t1:c.765+3A>T	NP_002991.2:n.765+3A>T
NM_003000.3:c.765+3A>T MANE Select	NP_002991.2:n.765+3A>T