Canonical Allele Identifier: CA338272434

Gene: SDHB

Linked Data

• ClinVar Variation Id: 1489328
• ClinVar RCV Id: RCV002001471
• dbSNP Id: rs2101521549
• MyVariant Identifiers: chr1:g.17354251T>A (hg19) ; chr1:g.17027756T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027756T>A , CM000663.2:g.17027756T>A	GRCh38
NC_000001.10:g.17354251T>A , CM000663.1:g.17354251T>A	GRCh37
NC_000001.9:g.17226838T>A	NCBI36
NG_012340.1:g.31415A>T , LRG_316:g.31415A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.362A>T	ENSP00000481376.2:p.Glu121Val
ENST00000491274.6:c.491A>T	ENSP00000480482.2:p.Glu164Val
ENST00000375499.8:c.533A>T MANE Select	ENSP00000364649.3:p.Glu178Val
ENST00000375499.7:c.533A>T	ENSP00000364649.3:p.Glu178Val
ENST00000463045.2:c.362A>T	ENSP00000481376.1:p.Glu121Val
ENST00000475506.1:n.450A>T
ENST00000485515.5:n.467A>T
ENST00000491274.5:c.491A>T	ENSP00000480482.1:p.Glu164Val
NM_003000.2:c.533A>T , LRG_316t1:c.533A>T	NP_002991.2:p.Glu178Val
NM_003000.3:c.533A>T MANE Select	NP_002991.2:p.Glu178Val