Canonical Allele Identifier: CA10608747
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 293808
ClinVar RCV Id: RCV000323643 RCV000380653
dbSNP Id: rs201155896
gnomAD v2: 1-17345274-T-C
gnomAD v3: 1-17018779-T-C
gnomAD v4: 1-17018779-T-C
MyVariant Identifiers: chr1:g.17345274T>C (hg19) chr1:g.17018779T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17018779T>C , CM000663.2:g.17018779T>C GRCh38
NC_000001.10:g.17345274T>C , CM000663.1:g.17345274T>C GRCh37
NC_000001.9:g.17217861T>C NCBI36
NG_012340.1:g.40392A>G , LRG_316:g.40392A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.*102A>G ENSP00000481376.2:n.*102A>G
ENST00000491274.6:c.*102A>G ENSP00000480482.2:n.*102A>G
ENST00000375499.8:c.*102A>G MANE Select ENSP00000364649.3:n.*102A>G
ENST00000375499.7:c.*102A>G ENSP00000364649.3:n.*102A>G
ENST00000475049.5:n.370A>G
ENST00000485092.5:n.609A>G
NM_003000.2:c.*102A>G , LRG_316t1:c.*102A>G NP_002991.2:n.*102A>G
NM_003000.3:c.*102A>G MANE Select NP_002991.2:n.*102A>G
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Search 100 bp 3'