Canonical Allele Identifier: CA915941150
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 662440
ClinVar RCV Id: RCV000820083
dbSNP Id: rs1570944850
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022669_17022720dup , CM000663.2:g.17022669_17022720dup GRCh38
NC_000001.10:g.17349164_17349215dup , CM000663.1:g.17349164_17349215dup GRCh37
NC_000001.9:g.17221751_17221802dup NCBI36
NG_012340.1:g.36454_36505dup , LRG_316:g.36454_36505dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.485_536dup ENSP00000481376.2:p.Pro180AspfsTer2
ENST00000491274.6:c.614_665dup ENSP00000480482.2:p.Pro223AspfsTer2
ENST00000375499.8:c.656_707dup MANE Select ENSP00000364649.3:p.Pro237AspfsTer2
ENST00000375499.7:c.656_707dup ENSP00000364649.3:p.Pro237AspfsTer2
ENST00000475049.5:n.81_132dup
ENST00000485092.5:n.320_371dup
ENST00000485515.5:n.590_641dup
NM_003000.2:c.656_707dup , LRG_316t1:c.656_707dup NP_002991.2:p.Pro237AspfsTer2
NM_003000.3:c.656_707dup MANE Select NP_002991.2:p.Pro237AspfsTer2
Search 100 bp 5'
Search 100 bp 3'