Canonical Allele Identifier: CA18662107
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 2041921
ClinVar RCV Id: RCV002903346
dbSNP Id: rs201832634
gnomAD v2: 1-17349094-C-A
gnomAD v4: 1-17022599-C-A
MyVariant Identifiers: chr1:g.17349094C>A (hg19) chr1:g.17022599C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022599C>A , CM000663.2:g.17022599C>A GRCh38
NC_000001.10:g.17349094C>A , CM000663.1:g.17349094C>A GRCh37
NC_000001.9:g.17221681C>A NCBI36
NG_012340.1:g.36572G>T , LRG_316:g.36572G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.594+9G>T ENSP00000481376.2:n.594+9G>T
ENST00000491274.6:c.723+9G>T ENSP00000480482.2:n.723+9G>T
ENST00000375499.8:c.765+9G>T MANE Select ENSP00000364649.3:n.765+9G>T
ENST00000375499.7:c.765+9G>T ENSP00000364649.3:n.765+9G>T
ENST00000475049.5:n.190+9G>T
ENST00000485092.5:n.429+9G>T
NM_003000.2:c.765+9G>T , LRG_316t1:c.765+9G>T NP_002991.2:n.765+9G>T
NM_003000.3:c.765+9G>T MANE Select NP_002991.2:n.765+9G>T
Search 100 bp 5'
Search 100 bp 3'