Canonical Allele Identifier: CA1156078099
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2077969989
gnomAD v4: 1-17022897-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022897C>T , CM000663.2:g.17022897C>T GRCh38
NC_000001.10:g.17349392C>T , CM000663.1:g.17349392C>T GRCh37
NC_000001.9:g.17221979C>T NCBI36
NG_012340.1:g.36274G>A , LRG_316:g.36274G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.472-167G>A ENSP00000481376.2:n.472-167G>A
ENST00000491274.6:c.601-167G>A ENSP00000480482.2:n.601-167G>A
ENST00000375499.8:c.643-167G>A MANE Select ENSP00000364649.3:n.643-167G>A
ENST00000375499.7:c.643-167G>A ENSP00000364649.3:n.643-167G>A
ENST00000475049.5:n.68-167G>A
ENST00000485092.5:n.140G>A
ENST00000485515.5:n.577-167G>A
NM_003000.2:c.643-167G>A , LRG_316t1:c.643-167G>A NP_002991.2:n.643-167G>A
NM_003000.3:c.643-167G>A MANE Select NP_002991.2:n.643-167G>A
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