Canonical Allele Identifier: CA999077718
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2077945131
gnomAD v3: 1-17018781-C-T
gnomAD v4: 1-17018781-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17018781C>T , CM000663.2:g.17018781C>T GRCh38
NC_000001.10:g.17345276C>T , CM000663.1:g.17345276C>T GRCh37
NC_000001.9:g.17217863C>T NCBI36
NG_012340.1:g.40390G>A , LRG_316:g.40390G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.*100G>A ENSP00000481376.2:n.*100G>A
ENST00000491274.6:c.*100G>A ENSP00000480482.2:n.*100G>A
ENST00000375499.8:c.*100G>A MANE Select ENSP00000364649.3:n.*100G>A
ENST00000375499.7:c.*100G>A ENSP00000364649.3:n.*100G>A
ENST00000475049.5:n.368G>A
ENST00000485092.5:n.607G>A
NM_003000.2:c.*100G>A , LRG_316t1:c.*100G>A NP_002991.2:n.*100G>A
NM_003000.3:c.*100G>A MANE Select NP_002991.2:n.*100G>A
Search 100 bp 5'
Search 100 bp 3'