Canonical Allele Identifier: CA2580060637
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 1996497
ClinVar RCV Id: RCV002823753
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028754T>C , CM000663.2:g.17028754T>C GRCh38
NC_000001.10:g.17355249T>C , CM000663.1:g.17355249T>C GRCh37
NC_000001.9:g.17227836T>C NCBI36
NG_012340.1:g.30417A>G , LRG_316:g.30417A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.116-18A>G ENSP00000481376.2:n.116-18A>G
ENST00000491274.6:c.245-18A>G ENSP00000480482.2:n.245-18A>G
ENST00000375499.8:c.287-18A>G MANE Select ENSP00000364649.3:n.287-18A>G
ENST00000375499.7:c.287-18A>G ENSP00000364649.3:n.287-18A>G
ENST00000463045.2:c.116-18A>G ENSP00000481376.1:n.116-18A>G
ENST00000475506.1:n.204-18A>G
ENST00000485515.5:n.275-18A>G
ENST00000491274.5:c.245-18A>G ENSP00000480482.1:n.245-18A>G
NM_003000.2:c.287-18A>G , LRG_316t1:c.287-18A>G NP_002991.2:n.287-18A>G
NM_003000.3:c.287-18A>G MANE Select NP_002991.2:n.287-18A>G
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