Canonical Allele Identifier: CA089588
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 656456
ClinVar RCV Id: RCV000812882 RCV001019384 RCV002268306 RCV003472416 RCV003151816 RCV004001747
dbSNP Id: rs767062764
ExAC: 1:17355195 C / T
gnomAD v2: 1-17355195-C-T
gnomAD v3: 1-17028700-C-T
gnomAD v4: 1-17028700-C-T
MyVariant Identifiers: chr1:g.17355195C>T (hg19) chr1:g.17028700C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028700C>T , CM000663.2:g.17028700C>T GRCh38
NC_000001.10:g.17355195C>T , CM000663.1:g.17355195C>T GRCh37
NC_000001.9:g.17227782C>T NCBI36
NG_012340.1:g.30471G>A , LRG_316:g.30471G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.152G>A ENSP00000481376.2:p.Gly51Asp
ENST00000491274.6:c.281G>A ENSP00000480482.2:p.Gly94Asp
ENST00000375499.8:c.323G>A MANE Select ENSP00000364649.3:p.Gly108Asp
ENST00000375499.7:c.323G>A ENSP00000364649.3:p.Gly108Asp
ENST00000463045.2:c.152G>A ENSP00000481376.1:p.Gly51Asp
ENST00000475506.1:n.240G>A
ENST00000485515.5:n.311G>A
ENST00000491274.5:c.281G>A ENSP00000480482.1:p.Gly94Asp
NM_003000.2:c.323G>A , LRG_316t1:c.323G>A NP_002991.2:p.Gly108Asp
NM_003000.3:c.323G>A MANE Select NP_002991.2:p.Gly108Asp
Search 100 bp 5'
Search 100 bp 3'