Canonical Allele Identifier: CA089700
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 760068
ClinVar RCV Id: RCV001477352
dbSNP Id: rs374921867
ExAC: 1:17349232 A / G
gnomAD v2: 1-17349232-A-G
gnomAD v3: 1-17022737-A-G
gnomAD v4: 1-17022737-A-G
MyVariant Identifiers: chr1:g.17349232A>G (hg19) chr1:g.17022737A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022737A>G , CM000663.2:g.17022737A>G GRCh38
NC_000001.10:g.17349232A>G , CM000663.1:g.17349232A>G GRCh37
NC_000001.9:g.17221819A>G NCBI36
NG_012340.1:g.36434T>C , LRG_316:g.36434T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.472-7T>C ENSP00000481376.2:n.472-7T>C
ENST00000491274.6:c.601-7T>C ENSP00000480482.2:n.601-7T>C
ENST00000375499.8:c.643-7T>C MANE Select ENSP00000364649.3:n.643-7T>C
ENST00000375499.7:c.643-7T>C ENSP00000364649.3:n.643-7T>C
ENST00000475049.5:n.68-7T>C
ENST00000485092.5:n.300T>C
ENST00000485515.5:n.577-7T>C
NM_003000.2:c.643-7T>C , LRG_316t1:c.643-7T>C NP_002991.2:n.643-7T>C
NM_003000.3:c.643-7T>C MANE Select NP_002991.2:n.643-7T>C
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