Canonical Allele Identifier: CA1156080551
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 1664633
ClinVar RCV Id: RCV002181799
dbSNP Id: rs2078005658
gnomAD v4: 1-17028752-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028752A>G , CM000663.2:g.17028752A>G GRCh38
NC_000001.10:g.17355247A>G , CM000663.1:g.17355247A>G GRCh37
NC_000001.9:g.17227834A>G NCBI36
NG_012340.1:g.30419T>C , LRG_316:g.30419T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.116-16T>C ENSP00000481376.2:n.116-16T>C
ENST00000491274.6:c.245-16T>C ENSP00000480482.2:n.245-16T>C
ENST00000375499.8:c.287-16T>C MANE Select ENSP00000364649.3:n.287-16T>C
ENST00000375499.7:c.287-16T>C ENSP00000364649.3:n.287-16T>C
ENST00000463045.2:c.116-16T>C ENSP00000481376.1:n.116-16T>C
ENST00000475506.1:n.204-16T>C
ENST00000485515.5:n.275-16T>C
ENST00000491274.5:c.245-16T>C ENSP00000480482.1:n.245-16T>C
NM_003000.2:c.287-16T>C , LRG_316t1:c.287-16T>C NP_002991.2:n.287-16T>C
NM_003000.3:c.287-16T>C MANE Select NP_002991.2:n.287-16T>C
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