Canonical Allele Identifier: CA915941160
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 766282
ClinVar RCV Id: RCV001467641
dbSNP Id: rs1570963404

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17053940G>C , CM000663.2:g.17053940G>C GRCh38
NC_000001.10:g.17380435G>C , CM000663.1:g.17380435G>C GRCh37
NC_000001.9:g.17253022G>C NCBI36
NG_012340.1:g.5231C>G , LRG_316:g.5231C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375499.8:c.72+8C>G MANE Select ENSP00000364649.3:n.72+8C>G
ENST00000375499.7:c.72+8C>G ENSP00000364649.3:n.72+8C>G
ENST00000466613.2:n.84+8C>G
ENST00000485515.5:n.60+8C>G
NM_003000.2:c.72+8C>G , LRG_316t1:c.72+8C>G NP_002991.2:n.72+8C>G
NM_003000.3:c.72+8C>G MANE Select NP_002991.2:n.72+8C>G