Canonical Allele Identifier: CA416082158
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 3223013
ClinVar RCV Id: RCV004508368
MyVariant Identifiers: chr1:g.17349217G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022722G>C , CM000663.2:g.17022722G>C GRCh38
NC_000001.10:g.17349217G>C , CM000663.1:g.17349217G>C GRCh37
NC_000001.9:g.17221804G>C NCBI36
NG_012340.1:g.36449C>G , LRG_316:g.36449C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.480C>G ENSP00000481376.2:p.Arg160=
ENST00000491274.6:c.609C>G ENSP00000480482.2:p.Arg203=
ENST00000375499.8:c.651C>G MANE Select ENSP00000364649.3:p.Arg217=
ENST00000375499.7:c.651C>G ENSP00000364649.3:p.Arg217=
ENST00000475049.5:n.76C>G
ENST00000485092.5:n.315C>G
ENST00000485515.5:n.585C>G
NM_003000.2:c.651C>G , LRG_316t1:c.651C>G NP_002991.2:p.Arg217=
NM_003000.3:c.651C>G MANE Select NP_002991.2:p.Arg217=