Canonical Allele Identifier: CA16609920
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 412454
ClinVar RCV Id: RCV000471748
dbSNP Id: rs1060503752
MyVariant Identifiers: chr1:g.17350489_17350490del (hg19) chr1:g.17023994_17023995del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17023994_17023995del , CM000663.2:g.17023994_17023995del GRCh38
NC_000001.10:g.17350489_17350490del , CM000663.1:g.17350489_17350490del GRCh37
NC_000001.9:g.17223076_17223077del NCBI36
NG_012340.1:g.35176_35177del , LRG_316:g.35176_35177del

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.449_450del ENSP00000481376.2:p.Leu150ArgfsTer14
ENST00000491274.6:c.578_579del ENSP00000480482.2:p.Leu193ArgfsTer14
ENST00000375499.8:c.620_621del MANE Select ENSP00000364649.3:p.Leu207ArgfsTer14
ENST00000375499.7:c.620_621del ENSP00000364649.3:p.Leu207ArgfsTer14
ENST00000485515.5:n.554_555del
ENST00000491274.5:c.578_579del ENSP00000480482.1:p.Leu193ArgfsTer?
NM_003000.2:c.620_621del , LRG_316t1:c.620_621del NP_002991.2:p.Leu207ArgfsTer14
NM_003000.3:c.620_621del MANE Select NP_002991.2:p.Leu207ArgfsTer14
Search 100 bp 5'
Search 100 bp 3'