Canonical Allele Identifier: CA1156080483
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028614T= , CM000663.2:g.17028614T= GRCh38
NC_000001.10:g.17355109T= , CM000663.1:g.17355109T= GRCh37
NC_000001.9:g.17227696T= NCBI36
NG_012340.1:g.30557A= , LRG_316:g.30557A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.238A= ENSP00000481376.2:p.Lys80=
ENST00000491274.6:c.367A= ENSP00000480482.2:p.Lys123=
ENST00000375499.8:c.409A= MANE Select ENSP00000364649.3:p.Lys137=
ENST00000375499.7:c.409A= ENSP00000364649.3:p.Lys137=
ENST00000463045.2:c.238A= ENSP00000481376.1:p.Lys80=
ENST00000475506.1:n.326A=
ENST00000485515.5:n.357+40A=
ENST00000491274.5:c.367A= ENSP00000480482.1:p.Lys123=
NM_003000.2:c.409A= , LRG_316t1:c.409A= NP_002991.2:p.Lys137=
NM_003000.3:c.409A= MANE Select NP_002991.2:p.Lys137=