Canonical Allele Identifier: CA015712
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 44642
ClinVar RCV Id: RCV000037719 RCV000128907 RCV000332692 RCV000478921 RCV000633965
dbSNP Id: rs397516833
MyVariant Identifiers: chr1:g.17355232C>G (hg19) chr1:g.17028737C>G (hg38)
PubMed: PMID:15328326 PMID:17200167 PMID:18382370 PMID:19454582 PMID:23072324 PMID:23512077 PMID:25371406 PMID:26302408 PMID:27549546
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028737C>G , CM000663.2:g.17028737C>G GRCh38
NC_000001.10:g.17355232C>G , CM000663.1:g.17355232C>G GRCh37
NC_000001.9:g.17227819C>G NCBI36
NG_012340.1:g.30434G>C , LRG_316:g.30434G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.116-1G>C ENSP00000481376.2:n.116-1G>C
ENST00000491274.6:c.245-1G>C ENSP00000480482.2:n.245-1G>C
ENST00000375499.8:c.287-1G>C MANE Select ENSP00000364649.3:n.287-1G>C
ENST00000375499.7:c.287-1G>C ENSP00000364649.3:n.287-1G>C
ENST00000463045.2:c.116-1G>C ENSP00000481376.1:n.116-1G>C
ENST00000475506.1:n.204-1G>C
ENST00000485515.5:n.275-1G>C
ENST00000491274.5:c.245-1G>C ENSP00000480482.1:n.245-1G>C
NM_003000.2:c.287-1G>C , LRG_316t1:c.287-1G>C NP_002991.2:n.287-1G>C
NM_003000.3:c.287-1G>C MANE Select NP_002991.2:n.287-1G>C
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