Canonical Allele Identifier: CA18659683
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs912733209

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17018772T>C , CM000663.2:g.17018772T>C GRCh38
NC_000001.10:g.17345267T>C , CM000663.1:g.17345267T>C GRCh37
NC_000001.9:g.17217854T>C NCBI36
NG_012340.1:g.40399A>G , LRG_316:g.40399A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.*109A>G ENSP00000481376.2:n.*109A>G
ENST00000491274.6:c.*109A>G ENSP00000480482.2:n.*109A>G
ENST00000375499.8:c.*109A>G MANE Select ENSP00000364649.3:n.*109A>G
ENST00000375499.7:c.*109A>G ENSP00000364649.3:n.*109A>G
ENST00000475049.5:n.377A>G
ENST00000485092.5:n.616A>G
NM_003000.2:c.*109A>G , LRG_316t1:c.*109A>G NP_002991.2:n.*109A>G
NM_003000.3:c.*109A>G MANE Select NP_002991.2:n.*109A>G