Canonical Allele Identifier: CA1156080488
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028627G= , CM000663.2:g.17028627G= GRCh38
NC_000001.10:g.17355122G= , CM000663.1:g.17355122G= GRCh37
NC_000001.9:g.17227709G= NCBI36
NG_012340.1:g.30544C= , LRG_316:g.30544C=

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.225C= ENSP00000481376.2:p.His75=
ENST00000491274.6:c.354C= ENSP00000480482.2:p.His118=
ENST00000375499.8:c.396C= MANE Select ENSP00000364649.3:p.His132=
ENST00000375499.7:c.396C= ENSP00000364649.3:p.His132=
ENST00000463045.2:c.225C= ENSP00000481376.1:p.His75=
ENST00000475506.1:n.313C=
ENST00000485515.5:n.357+27C=
ENST00000491274.5:c.354C= ENSP00000480482.1:p.His118=
NM_003000.2:c.396C= , LRG_316t1:c.396C= NP_002991.2:p.His132=
NM_003000.3:c.396C= MANE Select NP_002991.2:p.His132=