Canonical Allele Identifier: CA16609948
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 412474
dbSNP Id: rs1060503762

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17044820C>T , CM000663.2:g.17044820C>T GRCh38
NC_000001.10:g.17371315C>T , CM000663.1:g.17371315C>T GRCh37
NC_000001.9:g.17243902C>T NCBI36
NG_012340.1:g.14351G>A , LRG_316:g.14351G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.-31G>A ENSP00000481376.2:n.-31G>A
ENST00000491274.6:c.99G>A ENSP00000480482.2:p.Trp33Ter
ENST00000375499.8:c.141G>A MANE Select ENSP00000364649.3:p.Trp47Ter
ENST00000375499.7:c.141G>A ENSP00000364649.3:p.Trp47Ter
ENST00000463045.2:c.-31G>A ENSP00000481376.1:n.-31G>A
ENST00000466613.2:n.153G>A
ENST00000475506.1:n.58G>A
ENST00000485515.5:n.129G>A
ENST00000491274.5:c.99G>A ENSP00000480482.1:p.Trp33Ter
NM_003000.2:c.141G>A , LRG_316t1:c.141G>A NP_002991.2:p.Trp47Ter
NM_003000.3:c.141G>A MANE Select NP_002991.2:p.Trp47Ter