Canonical Allele Identifier: CA416048674
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 2948490
ClinVar RCV Id: RCV003809264
MyVariant Identifiers: chr1:g.17380448G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17053953G>A , CM000663.2:g.17053953G>A GRCh38
NC_000001.10:g.17380448G>A , CM000663.1:g.17380448G>A GRCh37
NC_000001.9:g.17253035G>A NCBI36
NG_012340.1:g.5218C>T , LRG_316:g.5218C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000375499.8:c.67C>T MANE Select ENSP00000364649.3:p.Leu23=
ENST00000375499.7:c.67C>T ENSP00000364649.3:p.Leu23=
ENST00000466613.2:n.79C>T
ENST00000485515.5:n.55C>T
NM_003000.2:c.67C>T , LRG_316t1:c.67C>T NP_002991.2:p.Leu23=
NM_003000.3:c.67C>T MANE Select NP_002991.2:p.Leu23=
Search 100 bp 5'
Search 100 bp 3'