Canonical Allele Identifier: CA089776
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 2014539
ClinVar RCV Id: RCV002830086
dbSNP Id: rs749662497
ExAC: 1:17371366 C / T
gnomAD v2: 1-17371366-C-T
gnomAD v4: 1-17044871-C-T
MyVariant Identifiers: chr1:g.17371366C>T (hg19) chr1:g.17044871C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17044871C>T , CM000663.2:g.17044871C>T GRCh38
NC_000001.10:g.17371366C>T , CM000663.1:g.17371366C>T GRCh37
NC_000001.9:g.17243953C>T NCBI36
NG_012340.1:g.14300G>A , LRG_316:g.14300G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.-82G>A ENSP00000481376.2:n.-82G>A
ENST00000491274.6:c.48G>A ENSP00000480482.2:p.Gln16=
ENST00000375499.8:c.90G>A MANE Select ENSP00000364649.3:p.Gln30=
ENST00000375499.7:c.90G>A ENSP00000364649.3:p.Gln30=
ENST00000463045.2:c.-82G>A ENSP00000481376.1:n.-82G>A
ENST00000466613.2:n.102G>A
ENST00000475506.1:n.7G>A
ENST00000485515.5:n.78G>A
ENST00000491274.5:c.48G>A ENSP00000480482.1:p.Gln16=
NM_003000.2:c.90G>A , LRG_316t1:c.90G>A NP_002991.2:p.Gln30=
NM_003000.3:c.90G>A MANE Select NP_002991.2:p.Gln30=
Search 100 bp 5'
Search 100 bp 3'