Canonical Allele Identifier: CA1140563935
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022315_17022317delinsGGG , CM000663.2:g.17022315_17022317delinsGGG GRCh38
NC_000001.10:g.17348810_17348812delinsGGG , CM000663.1:g.17348810_17348812delinsGGG GRCh37
NC_000001.9:g.17221397_17221399delinsGGG NCBI36
NG_012340.1:g.36854_36856delinsCCC , LRG_316:g.36854_36856delinsCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+291_594+293delinsCCC ENSP00000481376.2:n.594+291_594+293delinsCCC
ENST00000491274.6:c.723+291_723+293delinsCCC ENSP00000480482.2:n.723+291_723+293delinsCCC
ENST00000375499.8:c.765+291_765+293delinsCCC MANE Select ENSP00000364649.3:n.765+291_765+293delinsCCC
ENST00000375499.7:c.765+291_765+293delinsCCC ENSP00000364649.3:n.765+291_765+293delinsCCC
ENST00000475049.5:n.190+291_190+293delinsCCC
ENST00000485092.5:n.429+291_429+293delinsCCC
NM_003000.2:c.765+291_765+293delinsCCC , LRG_316t1:c.765+291_765+293delinsCCC NP_002991.2:n.765+291_765+293delinsCCC
NM_003000.3:c.765+291_765+293delinsCCC MANE Select NP_002991.2:n.765+291_765+293delinsCCC