Canonical Allele Identifier: CA2573130750
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 1671760
ClinVar RCV Id: RCV002199200
dbSNP Id: rs2101541285
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17044752G>T , CM000663.2:g.17044752G>T GRCh38
NC_000001.10:g.17371247G>T , CM000663.1:g.17371247G>T GRCh37
NC_000001.9:g.17243834G>T NCBI36
NG_012340.1:g.14419C>A , LRG_316:g.14419C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.29+9C>A ENSP00000481376.2:n.29+9C>A
ENST00000491274.6:c.158+9C>A ENSP00000480482.2:n.158+9C>A
ENST00000375499.8:c.200+9C>A MANE Select ENSP00000364649.3:n.200+9C>A
ENST00000375499.7:c.200+9C>A ENSP00000364649.3:n.200+9C>A
ENST00000463045.2:c.29+9C>A ENSP00000481376.1:n.29+9C>A
ENST00000466613.2:n.212+9C>A
ENST00000475506.1:n.117+9C>A
ENST00000485515.5:n.188+9C>A
ENST00000491274.5:c.158+9C>A ENSP00000480482.1:n.158+9C>A
NM_003000.2:c.200+9C>A , LRG_316t1:c.200+9C>A NP_002991.2:n.200+9C>A
NM_003000.3:c.200+9C>A MANE Select NP_002991.2:n.200+9C>A
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