Canonical Allele Identifier: CA338230595
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 664893
ClinVar RCV Id: RCV000823074
dbSNP Id: rs1570963430
MyVariant Identifiers: chr1:g.17380445G>A (hg19) chr1:g.17053950G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17053950G>A , CM000663.2:g.17053950G>A GRCh38
NC_000001.10:g.17380445G>A , CM000663.1:g.17380445G>A GRCh37
NC_000001.9:g.17253032G>A NCBI36
NG_012340.1:g.5221C>T , LRG_316:g.5221C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000375499.8:c.70C>T MANE Select ENSP00000364649.3:p.Gln24Ter
ENST00000375499.7:c.70C>T ENSP00000364649.3:p.Gln24Ter
ENST00000466613.2:n.82C>T
ENST00000485515.5:n.58C>T
NM_003000.2:c.70C>T , LRG_316t1:c.70C>T NP_002991.2:p.Gln24Ter
NM_003000.3:c.70C>T MANE Select NP_002991.2:p.Gln24Ter
Search 100 bp 5'
Search 100 bp 3'