Canonical Allele Identifier: CA1156080172
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027792C= , CM000663.2:g.17027792C= GRCh38
NC_000001.10:g.17354287C= , CM000663.1:g.17354287C= GRCh37
NC_000001.9:g.17226874C= NCBI36
NG_012340.1:g.31379G= , LRG_316:g.31379G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.326G= ENSP00000481376.2:p.Gly109=
ENST00000491274.6:c.455G= ENSP00000480482.2:p.Gly152=
ENST00000375499.8:c.497G= MANE Select ENSP00000364649.3:p.Gly166=
ENST00000375499.7:c.497G= ENSP00000364649.3:p.Gly166=
ENST00000463045.2:c.326G= ENSP00000481376.1:p.Gly109=
ENST00000475506.1:n.414G=
ENST00000485515.5:n.431G=
ENST00000491274.5:c.455G= ENSP00000480482.1:p.Gly152=
NM_003000.2:c.497G= , LRG_316t1:c.497G= NP_002991.2:p.Gly166=
NM_003000.3:c.497G= MANE Select NP_002991.2:p.Gly166=