Canonical Allele Identifier: CA1156077973
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022624G= , CM000663.2:g.17022624G= GRCh38
NC_000001.10:g.17349119G= , CM000663.1:g.17349119G= GRCh37
NC_000001.9:g.17221706G= NCBI36
NG_012340.1:g.36547C= , LRG_316:g.36547C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.578C= ENSP00000481376.2:p.Thr193=
ENST00000491274.6:c.707C= ENSP00000480482.2:p.Thr236=
ENST00000375499.8:c.749C= MANE Select ENSP00000364649.3:p.Thr250=
ENST00000375499.7:c.749C= ENSP00000364649.3:p.Thr250=
ENST00000475049.5:n.174C=
ENST00000485092.5:n.413C=
ENST00000485515.5:n.683C=
NM_003000.2:c.749C= , LRG_316t1:c.749C= NP_002991.2:p.Thr250=
NM_003000.3:c.749C= MANE Select NP_002991.2:p.Thr250=