Canonical Allele Identifier: CA015636
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 185809
dbSNP Id: rs74315366
gnomAD v4: 1-17033078-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17033078G>C , CM000663.2:g.17033078G>C GRCh38
NC_000001.10:g.17359573G>C , CM000663.1:g.17359573G>C GRCh37
NC_000001.9:g.17232160G>C NCBI36
NG_012340.1:g.26093C>G , LRG_316:g.26093C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.97C>G ENSP00000481376.2:p.Arg33Gly
ENST00000491274.6:c.226C>G ENSP00000480482.2:p.Arg76Gly
ENST00000375499.8:c.268C>G MANE Select ENSP00000364649.3:p.Arg90Gly
ENST00000375499.7:c.268C>G ENSP00000364649.3:p.Arg90Gly
ENST00000463045.2:c.97C>G ENSP00000481376.1:p.Arg33Gly
ENST00000466613.2:n.280C>G
ENST00000475506.1:n.185C>G
ENST00000485515.5:n.256C>G
ENST00000491274.5:c.226C>G ENSP00000480482.1:p.Arg76Gly
NM_003000.2:c.268C>G , LRG_316t1:c.268C>G NP_002991.2:p.Arg90Gly
NM_003000.3:c.268C>G MANE Select NP_002991.2:p.Arg90Gly