Canonical Allele Identifier: CA1156080170
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027788C= , CM000663.2:g.17027788C= GRCh38
NC_000001.10:g.17354283C= , CM000663.1:g.17354283C= GRCh37
NC_000001.9:g.17226870C= NCBI36
NG_012340.1:g.31383G= , LRG_316:g.31383G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.330G= ENSP00000481376.2:p.Lys110=
ENST00000491274.6:c.459G= ENSP00000480482.2:p.Lys153=
ENST00000375499.8:c.501G= MANE Select ENSP00000364649.3:p.Lys167=
ENST00000375499.7:c.501G= ENSP00000364649.3:p.Lys167=
ENST00000463045.2:c.330G= ENSP00000481376.1:p.Lys110=
ENST00000475506.1:n.418G=
ENST00000485515.5:n.435G=
ENST00000491274.5:c.459G= ENSP00000480482.1:p.Lys153=
NM_003000.2:c.501G= , LRG_316t1:c.501G= NP_002991.2:p.Lys167=
NM_003000.3:c.501G= MANE Select NP_002991.2:p.Lys167=