Canonical Allele Identifier: CA890985790
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs1429929153
gnomAD v3: 1-17023922-TC-T
gnomAD v4: 1-17023922-TC-T
MyVariant Identifiers: chr1:g.17350418del (hg19) chr1:g.17023923del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17023923del , CM000663.2:g.17023923del GRCh38
NC_000001.10:g.17350418del , CM000663.1:g.17350418del GRCh37
NC_000001.9:g.17223005del NCBI36
NG_012340.1:g.35248del , LRG_316:g.35248del

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.471+50del ENSP00000481376.2:n.471+50del
ENST00000491274.6:c.600+50del ENSP00000480482.2:n.600+50del
ENST00000375499.8:c.642+50del MANE Select ENSP00000364649.3:n.642+50del
ENST00000375499.7:c.642+50del ENSP00000364649.3:n.642+50del
ENST00000485515.5:n.576+50del
NM_003000.2:c.642+50del , LRG_316t1:c.642+50del NP_002991.2:n.642+50del
NM_003000.3:c.642+50del MANE Select NP_002991.2:n.642+50del
Search 100 bp 5'
Search 100 bp 3'