Canonical Allele Identifier: CA10577674
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 229669
ClinVar RCV Id: RCV000221754
dbSNP Id: rs876658132
MyVariant Identifiers: chr1:g.17354234_17354240del (hg19) chr1:g.17027739_17027745del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027742_17027748del , CM000663.2:g.17027742_17027748del GRCh38
NC_000001.10:g.17354237_17354243del , CM000663.1:g.17354237_17354243del GRCh37
NC_000001.9:g.17226824_17226830del NCBI36
NG_012340.1:g.31426_31432del , LRG_316:g.31426_31432del

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.369+4_369+10del ENSP00000481376.2:n.369+4_369+10del
ENST00000491274.6:c.498+4_498+10del ENSP00000480482.2:n.498+4_498+10del
ENST00000375499.8:c.540+4_540+10del MANE Select ENSP00000364649.3:n.540+4_540+10del
ENST00000375499.7:c.540+4_540+10del ENSP00000364649.3:n.540+4_540+10del
ENST00000475506.1:n.461_467del
ENST00000485515.5:n.474+4_474+10del
ENST00000491274.5:c.498+4_498+10del ENSP00000480482.1:n.498+4_498+10del
NM_003000.2:c.540+4_540+10del , LRG_316t1:c.540+4_540+10del NP_002991.2:n.540+4_540+10del
NM_003000.3:c.540+4_540+10del MANE Select NP_002991.2:n.540+4_540+10del
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