Canonical Allele Identifier: CA1156077790
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022189_17022191delinsAGC , CM000663.2:g.17022189_17022191delinsAGC GRCh38
NC_000001.10:g.17348684_17348686delinsAGC , CM000663.1:g.17348684_17348686delinsAGC GRCh37
NC_000001.9:g.17221271_17221273delinsAGC NCBI36
NG_012340.1:g.36980_36982delinsGCT , LRG_316:g.36980_36982delinsGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+417_594+419delinsGCT ENSP00000481376.2:n.594+417_594+419delinsGCT
ENST00000491274.6:c.723+417_723+419delinsGCT ENSP00000480482.2:n.723+417_723+419delinsGCT
ENST00000375499.8:c.765+417_765+419delinsGCT MANE Select ENSP00000364649.3:n.765+417_765+419delinsGCT
ENST00000375499.7:c.765+417_765+419delinsGCT ENSP00000364649.3:n.765+417_765+419delinsGCT
ENST00000475049.5:n.190+417_190+419delinsGCT
ENST00000485092.5:n.429+417_429+419delinsGCT
NM_003000.2:c.765+417_765+419delinsGCT , LRG_316t1:c.765+417_765+419delinsGCT NP_002991.2:n.765+417_765+419delinsGCT
NM_003000.3:c.765+417_765+419delinsGCT MANE Select NP_002991.2:n.765+417_765+419delinsGCT