Canonical Allele Identifier: CA2580060649
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 1753912
ClinVar RCV Id: RCV002364143

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17053939_17053962del , CM000663.2:g.17053939_17053962del GRCh38
NC_000001.10:g.17380434_17380457del , CM000663.1:g.17380434_17380457del GRCh37
NC_000001.9:g.17253021_17253044del NCBI36
NG_012340.1:g.5216_5239del , LRG_316:g.5216_5239del

Transcript Alleles

HGVS Amino-acid change
ENST00000375499.8:c.65_72+16del
ENST00000375499.7:c.65_72+16del
ENST00000466613.2:n.77_84+16del
ENST00000485515.5:n.53_60+16del
NM_003000.2:c.65_72+16del , LRG_316t1:c.65_72+16del
NM_003000.3:c.65_72+16del