Canonical Allele Identifier: CA1156077852
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs1177785742
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022342A>T , CM000663.2:g.17022342A>T GRCh38
NC_000001.10:g.17348837A>T , CM000663.1:g.17348837A>T GRCh37
NC_000001.9:g.17221424A>T NCBI36
NG_012340.1:g.36829T>A , LRG_316:g.36829T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+266T>A ENSP00000481376.2:n.594+266T>A
ENST00000491274.6:c.723+266T>A ENSP00000480482.2:n.723+266T>A
ENST00000375499.8:c.765+266T>A MANE Select ENSP00000364649.3:n.765+266T>A
ENST00000375499.7:c.765+266T>A ENSP00000364649.3:n.765+266T>A
ENST00000475049.5:n.190+266T>A
ENST00000485092.5:n.429+266T>A
NM_003000.2:c.765+266T>A , LRG_316t1:c.765+266T>A NP_002991.2:n.765+266T>A
NM_003000.3:c.765+266T>A MANE Select NP_002991.2:n.765+266T>A
Search 100 bp 5'
Search 100 bp 3'