Canonical Allele Identifier: CA645671465
Gene: SDHB HGNC NCBI

Linked Data

gnomAD v4: 1-17027616-A-C
COSMIC: COSN18003307
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027616A>C , CM000663.2:g.17027616A>C GRCh38
NC_000001.10:g.17354111A>C , CM000663.1:g.17354111A>C GRCh37
NC_000001.9:g.17226698A>C NCBI36
NG_012340.1:g.31555T>G , LRG_316:g.31555T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.369+133T>G ENSP00000481376.2:n.369+133T>G
ENST00000491274.6:c.498+133T>G ENSP00000480482.2:n.498+133T>G
ENST00000375499.8:c.540+133T>G MANE Select ENSP00000364649.3:n.540+133T>G
ENST00000375499.7:c.540+133T>G ENSP00000364649.3:n.540+133T>G
ENST00000485515.5:n.474+133T>G
ENST00000491274.5:c.498+133T>G ENSP00000480482.1:n.498+133T>G
NM_003000.2:c.540+133T>G , LRG_316t1:c.540+133T>G NP_002991.2:n.540+133T>G
NM_003000.3:c.540+133T>G MANE Select NP_002991.2:n.540+133T>G
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