Canonical Allele Identifier: CA338270115
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 1005286
ClinVar RCV Id: RCV001302135
dbSNP Id: rs1570944778
MyVariant Identifiers: chr1:g.17349131A>C (hg19) chr1:g.17022636A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022636A>C , CM000663.2:g.17022636A>C GRCh38
NC_000001.10:g.17349131A>C , CM000663.1:g.17349131A>C GRCh37
NC_000001.9:g.17221718A>C NCBI36
NG_012340.1:g.36535T>G , LRG_316:g.36535T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.566T>G ENSP00000481376.2:p.Ile189Ser
ENST00000491274.6:c.695T>G ENSP00000480482.2:p.Ile232Ser
ENST00000375499.8:c.737T>G MANE Select ENSP00000364649.3:p.Ile246Ser
ENST00000375499.7:c.737T>G ENSP00000364649.3:p.Ile246Ser
ENST00000475049.5:n.162T>G
ENST00000485092.5:n.401T>G
ENST00000485515.5:n.671T>G
NM_003000.2:c.737T>G , LRG_316t1:c.737T>G NP_002991.2:p.Ile246Ser
NM_003000.3:c.737T>G MANE Select NP_002991.2:p.Ile246Ser
Search 100 bp 5'
Search 100 bp 3'