Canonical Allele Identifier: CA2643675661
Gene: SDHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022601_17022602insTGGATTCAG , CM000663.2:g.17022601_17022602insTGGATTCAG GRCh38
NC_000001.10:g.17349096_17349097insTGGATTCAG , CM000663.1:g.17349096_17349097insTGGATTCAG GRCh37
NC_000001.9:g.17221683_17221684insTGGATTCAG NCBI36
NG_012340.1:g.36569_36570insCTGAATCCA , LRG_316:g.36569_36570insCTGAATCCA

Transcript Alleles

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