Canonical Allele Identifier: CA338228395
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 2625092
ClinVar RCV Id: RCV003377771

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17044878C>A , CM000663.2:g.17044878C>A GRCh38
NC_000001.10:g.17371373C>A , CM000663.1:g.17371373C>A GRCh37
NC_000001.9:g.17243960C>A NCBI36
NG_012340.1:g.14293G>T , LRG_316:g.14293G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.-89G>T ENSP00000481376.2:n.-89G>T
ENST00000491274.6:c.41G>T ENSP00000480482.2:p.Gly14Val
ENST00000375499.8:c.83G>T MANE Select ENSP00000364649.3:p.Gly28Val
ENST00000375499.7:c.83G>T ENSP00000364649.3:p.Gly28Val
ENST00000463045.2:c.-89G>T ENSP00000481376.1:n.-89G>T
ENST00000466613.2:n.95G>T
ENST00000485515.5:n.71G>T
ENST00000491274.5:c.41G>T ENSP00000480482.1:p.Gly14Val
NM_003000.2:c.83G>T , LRG_316t1:c.83G>T NP_002991.2:p.Gly28Val
NM_003000.3:c.83G>T MANE Select NP_002991.2:p.Gly28Val