Canonical Allele Identifier: CA915941149
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 642502
ClinVar RCV Id: RCV000795978
dbSNP Id: rs776039903
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022604G>T , CM000663.2:g.17022604G>T GRCh38
NC_000001.10:g.17349099G>T , CM000663.1:g.17349099G>T GRCh37
NC_000001.9:g.17221686G>T NCBI36
NG_012340.1:g.36567C>A , LRG_316:g.36567C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+4C>A ENSP00000481376.2:n.594+4C>A
ENST00000491274.6:c.723+4C>A ENSP00000480482.2:n.723+4C>A
ENST00000375499.8:c.765+4C>A MANE Select ENSP00000364649.3:n.765+4C>A
ENST00000375499.7:c.765+4C>A ENSP00000364649.3:n.765+4C>A
ENST00000475049.5:n.190+4C>A
ENST00000485092.5:n.429+4C>A
NM_003000.2:c.765+4C>A , LRG_316t1:c.765+4C>A NP_002991.2:n.765+4C>A
NM_003000.3:c.765+4C>A MANE Select NP_002991.2:n.765+4C>A
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