Canonical Allele Identifier: CA1156077931
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022535_17022537delinsCCT , CM000663.2:g.17022535_17022537delinsCCT GRCh38
NC_000001.10:g.17349030_17349032delinsCCT , CM000663.1:g.17349030_17349032delinsCCT GRCh37
NC_000001.9:g.17221617_17221619delinsCCT NCBI36
NG_012340.1:g.36634_36636delinsAGG , LRG_316:g.36634_36636delinsAGG

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.594+71_594+73delinsAGG ENSP00000481376.2:n.594+71_594+73delinsAG...
ENST00000491274.6:c.723+71_723+73delinsAGG ENSP00000480482.2:n.723+71_723+73delinsAG...
ENST00000375499.8:c.765+71_765+73delinsAGG MANE Select ENSP00000364649.3:n.765+71_765+73delinsAG...
ENST00000375499.7:c.765+71_765+73delinsAGG ENSP00000364649.3:n.765+71_765+73delinsAG...
ENST00000475049.5:n.190+71_190+73delinsAGG
ENST00000485092.5:n.429+71_429+73delinsAGG
NM_003000.2:c.765+71_765+73delinsAGG , LRG_316t1:c.765+71_765+73delinsAGG NP_002991.2:n.765+71_765+73delinsAGG
NM_003000.3:c.765+71_765+73delinsAGG MANE Select NP_002991.2:n.765+71_765+73delinsAGG