Canonical Allele Identifier: CA1156090997
Gene: SDHB HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.-31G= ENSP00000481376.2:n.-31G=
ENST00000491274.6:c.99G= ENSP00000480482.2:p.Trp33=
ENST00000375499.8:c.141G= MANE Select ENSP00000364649.3:p.Trp47=
ENST00000375499.7:c.141G= ENSP00000364649.3:p.Trp47=
ENST00000463045.2:c.-31G= ENSP00000481376.1:n.-31G=
ENST00000466613.2:n.153G=
ENST00000475506.1:n.58G=
ENST00000485515.5:n.129G=
ENST00000491274.5:c.99G= ENSP00000480482.1:p.Trp33=
NM_003000.2:c.141G= , LRG_316t1:c.141G= NP_002991.2:p.Trp47=
NM_003000.3:c.141G= MANE Select NP_002991.2:p.Trp47=