Canonical Allele Identifier: CA10577677
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 233346
ClinVar RCV Id: RCV000222005 RCV000938642
dbSNP Id: rs876660346
gnomAD v3: 1-17028711-G-A
gnomAD v4: 1-17028711-G-A
MyVariant Identifiers: chr1:g.17355206G>A (hg19) chr1:g.17028711G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028711G>A , CM000663.2:g.17028711G>A GRCh38
NC_000001.10:g.17355206G>A , CM000663.1:g.17355206G>A GRCh37
NC_000001.9:g.17227793G>A NCBI36
NG_012340.1:g.30460C>T , LRG_316:g.30460C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.141C>T ENSP00000481376.2:p.Asn47=
ENST00000491274.6:c.270C>T ENSP00000480482.2:p.Asn90=
ENST00000375499.8:c.312C>T MANE Select ENSP00000364649.3:p.Asn104=
ENST00000375499.7:c.312C>T ENSP00000364649.3:p.Asn104=
ENST00000463045.2:c.141C>T ENSP00000481376.1:p.Asn47=
ENST00000475506.1:n.229C>T
ENST00000485515.5:n.300C>T
ENST00000491274.5:c.270C>T ENSP00000480482.1:p.Asn90=
NM_003000.2:c.312C>T , LRG_316t1:c.312C>T NP_002991.2:p.Asn104=
NM_003000.3:c.312C>T MANE Select NP_002991.2:p.Asn104=
Search 100 bp 5'
Search 100 bp 3'