Canonical Allele Identifier: CA521037814
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs1450843616
gnomAD v2: 1-17349492-AT-A
gnomAD v3: 1-17022997-AT-A
gnomAD v4: 1-17022997-AT-A
MyVariant Identifiers: chr1:g.17349493del (hg19) chr1:g.17022998del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022999del , CM000663.2:g.17022999del GRCh38
NC_000001.10:g.17349494del , CM000663.1:g.17349494del GRCh37
NC_000001.9:g.17222081del NCBI36
NG_012340.1:g.36173del , LRG_316:g.36173del

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.472-268del ENSP00000481376.2:n.472-268del
ENST00000491274.6:c.601-268del ENSP00000480482.2:n.601-268del
ENST00000375499.8:c.643-268del MANE Select ENSP00000364649.3:n.643-268del
ENST00000375499.7:c.643-268del ENSP00000364649.3:n.643-268del
ENST00000475049.5:n.67+96del
ENST00000485092.5:n.39del
ENST00000485515.5:n.577-268del
NM_003000.2:c.643-268del , LRG_316t1:c.643-268del NP_002991.2:n.643-268del
NM_003000.3:c.643-268del MANE Select NP_002991.2:n.643-268del
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