Canonical Allele Identifier: CA16609934
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 412456
ClinVar RCV Id: RCV000463782
dbSNP Id: rs1060503753
MyVariant Identifiers: chr1:g.17354285T>A (hg19) chr1:g.17027790T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027790T>A , CM000663.2:g.17027790T>A GRCh38
NC_000001.10:g.17354285T>A , CM000663.1:g.17354285T>A GRCh37
NC_000001.9:g.17226872T>A NCBI36
NG_012340.1:g.31381A>T , LRG_316:g.31381A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.328A>T ENSP00000481376.2:p.Lys110Ter
ENST00000491274.6:c.457A>T ENSP00000480482.2:p.Lys153Ter
ENST00000375499.8:c.499A>T MANE Select ENSP00000364649.3:p.Lys167Ter
ENST00000375499.7:c.499A>T ENSP00000364649.3:p.Lys167Ter
ENST00000463045.2:c.328A>T ENSP00000481376.1:p.Lys110Ter
ENST00000475506.1:n.416A>T
ENST00000485515.5:n.433A>T
ENST00000491274.5:c.457A>T ENSP00000480482.1:p.Lys153Ter
NM_003000.2:c.499A>T , LRG_316t1:c.499A>T NP_002991.2:p.Lys167Ter
NM_003000.3:c.499A>T MANE Select NP_002991.2:p.Lys167Ter
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