Canonical Allele Identifier: CA890984854
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs1319850035
gnomAD v3: 1-17022535-CCT-C
gnomAD v4: 1-17022535-CCT-C
MyVariant Identifiers: chr1:g.17349031_17349032del (hg19) chr1:g.17022536_17022537del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022538_17022539del , CM000663.2:g.17022538_17022539del GRCh38
NC_000001.10:g.17349033_17349034del , CM000663.1:g.17349033_17349034del GRCh37
NC_000001.9:g.17221620_17221621del NCBI36
NG_012340.1:g.36634_36635del , LRG_316:g.36634_36635del

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.594+71_594+72del ENSP00000481376.2:n.594+71_594+72del
ENST00000491274.6:c.723+71_723+72del ENSP00000480482.2:n.723+71_723+72del
ENST00000375499.8:c.765+71_765+72del MANE Select ENSP00000364649.3:n.765+71_765+72del
ENST00000375499.7:c.765+71_765+72del ENSP00000364649.3:n.765+71_765+72del
ENST00000475049.5:n.190+71_190+72del
ENST00000485092.5:n.429+71_429+72del
NM_003000.2:c.765+71_765+72del , LRG_316t1:c.765+71_765+72del NP_002991.2:n.765+71_765+72del
NM_003000.3:c.765+71_765+72del MANE Select NP_002991.2:n.765+71_765+72del
Search 100 bp 5'
Search 100 bp 3'