Canonical Allele Identifier: CA1148443641
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17044873_17044875delinsGGG , CM000663.2:g.17044873_17044875delinsGGG GRCh38
NC_000001.10:g.17371368_17371370delinsGGG , CM000663.1:g.17371368_17371370delinsGGG GRCh37
NC_000001.9:g.17243955_17243957delinsGGG NCBI36
NG_012340.1:g.14296_14298delinsCCC , LRG_316:g.14296_14298delinsCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.-86_-84delinsCCC ENSP00000481376.2:n.-86_-84delinsCCC
ENST00000491274.6:c.44_46delinsCCC ENSP00000480482.2:p.Ala15=
ENST00000375499.8:c.86_88delinsCCC MANE Select ENSP00000364649.3:p.Ala29=
ENST00000375499.7:c.86_88delinsCCC ENSP00000364649.3:p.Ala29=
ENST00000463045.2:c.-86_-84delinsCCC ENSP00000481376.1:n.-86_-84delinsCCC
ENST00000466613.2:n.98_100delinsCCC
ENST00000475506.1:n.3_5delinsCCC
ENST00000485515.5:n.74_76delinsCCC
ENST00000491274.5:c.44_46delinsCCC ENSP00000480482.1:p.Ala15=
NM_003000.2:c.86_88delinsCCC , LRG_316t1:c.86_88delinsCCC NP_002991.2:p.Ala29=
NM_003000.3:c.86_88delinsCCC MANE Select NP_002991.2:p.Ala29=