Canonical Allele Identifier: CA1156080100
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2077998293

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027619del , CM000663.2:g.17027619del GRCh38
NC_000001.10:g.17354114del , CM000663.1:g.17354114del GRCh37
NC_000001.9:g.17226701del NCBI36
NG_012340.1:g.31554del , LRG_316:g.31554del

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.369+132del ENSP00000481376.2:n.369+132del
ENST00000491274.6:c.498+132del ENSP00000480482.2:n.498+132del
ENST00000375499.8:c.540+132del MANE Select ENSP00000364649.3:n.540+132del
ENST00000375499.7:c.540+132del ENSP00000364649.3:n.540+132del
ENST00000485515.5:n.474+132del
ENST00000491274.5:c.498+132del ENSP00000480482.1:n.498+132del
NM_003000.2:c.540+132del , LRG_316t1:c.540+132del NP_002991.2:n.540+132del
NM_003000.3:c.540+132del MANE Select NP_002991.2:n.540+132del