Canonical Allele Identifier: CA1156080325
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2078001821

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028147T>G , CM000663.2:g.17028147T>G GRCh38
NC_000001.10:g.17354642T>G , CM000663.1:g.17354642T>G GRCh37
NC_000001.9:g.17227229T>G NCBI36
NG_012340.1:g.31024A>C , LRG_316:g.31024A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.253-282A>C ENSP00000481376.2:n.253-282A>C
ENST00000491274.6:c.382-282A>C ENSP00000480482.2:n.382-282A>C
ENST00000375499.8:c.424-282A>C MANE Select ENSP00000364649.3:n.424-282A>C
ENST00000375499.7:c.424-282A>C ENSP00000364649.3:n.424-282A>C
ENST00000463045.2:c.253-282A>C ENSP00000481376.1:n.253-282A>C
ENST00000475506.1:n.341-282A>C
ENST00000485515.5:n.358-282A>C
ENST00000491274.5:c.382-282A>C ENSP00000480482.1:n.382-282A>C
NM_003000.2:c.424-282A>C , LRG_316t1:c.424-282A>C NP_002991.2:n.424-282A>C
NM_003000.3:c.424-282A>C MANE Select NP_002991.2:n.424-282A>C