Canonical Allele Identifier: CA1156077970
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022618G= , CM000663.2:g.17022618G= GRCh38
NC_000001.10:g.17349113G= , CM000663.1:g.17349113G= GRCh37
NC_000001.9:g.17221700G= NCBI36
NG_012340.1:g.36553C= , LRG_316:g.36553C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.584C= ENSP00000481376.2:p.Thr195=
ENST00000491274.6:c.713C= ENSP00000480482.2:p.Thr238=
ENST00000375499.8:c.755C= MANE Select ENSP00000364649.3:p.Thr252=
ENST00000375499.7:c.755C= ENSP00000364649.3:p.Thr252=
ENST00000475049.5:n.180C=
ENST00000485092.5:n.419C=
ENST00000485515.5:n.689C=
NM_003000.2:c.755C= , LRG_316t1:c.755C= NP_002991.2:p.Thr252=
NM_003000.3:c.755C= MANE Select NP_002991.2:p.Thr252=