Canonical Allele Identifier: CA890984822
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs1170569879
gnomAD v3: 1-17022458-CT-C
gnomAD v4: 1-17022458-CT-C
MyVariant Identifiers: chr1:g.17348954del (hg19) chr1:g.17022459del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022459del , CM000663.2:g.17022459del GRCh38
NC_000001.10:g.17348954del , CM000663.1:g.17348954del GRCh37
NC_000001.9:g.17221541del NCBI36
NG_012340.1:g.36712del , LRG_316:g.36712del

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+149del ENSP00000481376.2:n.594+149del
ENST00000491274.6:c.723+149del ENSP00000480482.2:n.723+149del
ENST00000375499.8:c.765+149del MANE Select ENSP00000364649.3:n.765+149del
ENST00000375499.7:c.765+149del ENSP00000364649.3:n.765+149del
ENST00000475049.5:n.190+149del
ENST00000485092.5:n.429+149del
NM_003000.2:c.765+149del , LRG_316t1:c.765+149del NP_002991.2:n.765+149del
NM_003000.3:c.765+149del MANE Select NP_002991.2:n.765+149del
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