Canonical Allele Identifier: CA2574234585
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 2930025
ClinVar RCV Id: RCV003787383
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022588G>A , CM000663.2:g.17022588G>A GRCh38
NC_000001.10:g.17349083G>A , CM000663.1:g.17349083G>A GRCh37
NC_000001.9:g.17221670G>A NCBI36
NG_012340.1:g.36583C>T , LRG_316:g.36583C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.594+20C>T ENSP00000481376.2:n.594+20C>T
ENST00000491274.6:c.723+20C>T ENSP00000480482.2:n.723+20C>T
ENST00000375499.8:c.765+20C>T MANE Select ENSP00000364649.3:n.765+20C>T
ENST00000375499.7:c.765+20C>T ENSP00000364649.3:n.765+20C>T
ENST00000475049.5:n.190+20C>T
ENST00000485092.5:n.429+20C>T
NM_003000.2:c.765+20C>T , LRG_316t1:c.765+20C>T NP_002991.2:n.765+20C>T
NM_003000.3:c.765+20C>T MANE Select NP_002991.2:n.765+20C>T
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