Canonical Allele Identifier: CA2574235850
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028509_17028512del , CM000663.2:g.17028509_17028512del GRCh38
NC_000001.10:g.17355004_17355007del , CM000663.1:g.17355004_17355007del GRCh37
NC_000001.9:g.17227591_17227594del NCBI36
NG_012340.1:g.30663_30666del , LRG_316:g.30663_30666del

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.252+92_252+95del ENSP00000481376.2:n.252+92_252+95del
ENST00000491274.6:c.381+92_381+95del ENSP00000480482.2:n.381+92_381+95del
ENST00000375499.8:c.423+92_423+95del MANE Select ENSP00000364649.3:n.423+92_423+95del
ENST00000375499.7:c.423+92_423+95del ENSP00000364649.3:n.423+92_423+95del
ENST00000463045.2:c.252+92_252+95del ENSP00000481376.1:n.252+92_252+95del
ENST00000475506.1:n.340+92_340+95del
ENST00000485515.5:n.357+146_357+149del
ENST00000491274.5:c.381+92_381+95del ENSP00000480482.1:n.381+92_381+95del
NM_003000.2:c.423+92_423+95del , LRG_316t1:c.423+92_423+95del NP_002991.2:n.423+92_423+95del
NM_003000.3:c.423+92_423+95del MANE Select NP_002991.2:n.423+92_423+95del