Canonical Allele Identifier: CA2574235877
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2101522850

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028567T>C , CM000663.2:g.17028567T>C GRCh38
NC_000001.10:g.17355062T>C , CM000663.1:g.17355062T>C GRCh37
NC_000001.9:g.17227649T>C NCBI36
NG_012340.1:g.30604A>G , LRG_316:g.30604A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.252+33A>G ENSP00000481376.2:n.252+33A>G
ENST00000491274.6:c.381+33A>G ENSP00000480482.2:n.381+33A>G
ENST00000375499.8:c.423+33A>G MANE Select ENSP00000364649.3:n.423+33A>G
ENST00000375499.7:c.423+33A>G ENSP00000364649.3:n.423+33A>G
ENST00000463045.2:c.252+33A>G ENSP00000481376.1:n.252+33A>G
ENST00000475506.1:n.340+33A>G
ENST00000485515.5:n.357+87A>G
ENST00000491274.5:c.381+33A>G ENSP00000480482.1:n.381+33A>G
NM_003000.2:c.423+33A>G , LRG_316t1:c.423+33A>G NP_002991.2:n.423+33A>G
NM_003000.3:c.423+33A>G MANE Select NP_002991.2:n.423+33A>G