Canonical Allele Identifier: CA338230587
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 1040802
ClinVar RCV Id: RCV001344511 RCV002377462
dbSNP Id: rs878854580
MyVariant Identifiers: chr1:g.17380444T>C (hg19) chr1:g.17053949T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17053949T>C , CM000663.2:g.17053949T>C GRCh38
NC_000001.10:g.17380444T>C , CM000663.1:g.17380444T>C GRCh37
NC_000001.9:g.17253031T>C NCBI36
NG_012340.1:g.5222A>G , LRG_316:g.5222A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375499.8:c.71A>G MANE Select ENSP00000364649.3:p.Gln24Arg
ENST00000375499.7:c.71A>G ENSP00000364649.3:p.Gln24Arg
ENST00000466613.2:n.83A>G
ENST00000485515.5:n.59A>G
NM_003000.2:c.71A>G , LRG_316t1:c.71A>G NP_002991.2:p.Gln24Arg
NM_003000.3:c.71A>G MANE Select NP_002991.2:p.Gln24Arg
Search 100 bp 5'
Search 100 bp 3'