Canonical Allele Identifier: CA916081285
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 839853
dbSNP Id: rs2078163018

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17053948_17053949delinsGG , CM000663.2:g.17053948_17053949delinsGG GRCh38
NC_000001.10:g.17380443_17380444delinsGG , CM000663.1:g.17380443_17380444delinsGG GRCh37
NC_000001.9:g.17253030_17253031delinsGG NCBI36
NG_012340.1:g.5222_5223delinsCC , LRG_316:g.5222_5223delinsCC

Transcript Alleles

HGVS Amino-acid change
ENST00000375499.8:c.71_72delinsCC MANE Select ENSP00000364649.3:p.Gln24Pro
ENST00000375499.7:c.71_72delinsCC ENSP00000364649.3:p.Gln24Pro
ENST00000466613.2:n.83_84delinsCC
ENST00000485515.5:n.59_60delinsCC
NM_003000.2:c.71_72delinsCC , LRG_316t1:c.71_72delinsCC NP_002991.2:p.Gln24Pro
NM_003000.3:c.71_72delinsCC MANE Select NP_002991.2:p.Gln24Pro