Canonical Allele Identifier: CA1156080311
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028127_17028130delinsACAC , CM000663.2:g.17028127_17028130delinsACAC GRCh38
NC_000001.10:g.17354622_17354625delinsACAC , CM000663.1:g.17354622_17354625delinsACAC GRCh37
NC_000001.9:g.17227209_17227212delinsACAC NCBI36
NG_012340.1:g.31041_31044delinsGTGT , LRG_316:g.31041_31044delinsGTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.253-265_253-262delinsGTGT ENSP00000481376.2:n.253-265_253-262delinsGTGT
ENST00000491274.6:c.382-265_382-262delinsGTGT ENSP00000480482.2:n.382-265_382-262delinsGTGT
ENST00000375499.8:c.424-265_424-262delinsGTGT MANE Select ENSP00000364649.3:n.424-265_424-262delinsGTGT
ENST00000375499.7:c.424-265_424-262delinsGTGT ENSP00000364649.3:n.424-265_424-262delinsGTGT
ENST00000463045.2:c.253-265_253-262delinsGTGT ENSP00000481376.1:n.253-265_253-262delinsGTGT
ENST00000475506.1:n.341-265_341-262delinsGTGT
ENST00000485515.5:n.358-265_358-262delinsGTGT
ENST00000491274.5:c.382-265_382-262delinsGTGT ENSP00000480482.1:n.382-265_382-262delinsGTGT
NM_003000.2:c.424-265_424-262delinsGTGT , LRG_316t1:c.424-265_424-262delinsGTGT NP_002991.2:n.424-265_424-262delinsGTGT
NM_003000.3:c.424-265_424-262delinsGTGT MANE Select NP_002991.2:n.424-265_424-262delinsGTGT