Canonical Allele Identifier: CA1156078579
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2077976862
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17023912C>T , CM000663.2:g.17023912C>T GRCh38
NC_000001.10:g.17350407C>T , CM000663.1:g.17350407C>T GRCh37
NC_000001.9:g.17222994C>T NCBI36
NG_012340.1:g.35259G>A , LRG_316:g.35259G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.471+61G>A ENSP00000481376.2:n.471+61G>A
ENST00000491274.6:c.600+61G>A ENSP00000480482.2:n.600+61G>A
ENST00000375499.8:c.642+61G>A MANE Select ENSP00000364649.3:n.642+61G>A
ENST00000375499.7:c.642+61G>A ENSP00000364649.3:n.642+61G>A
ENST00000485515.5:n.576+61G>A
NM_003000.2:c.642+61G>A , LRG_316t1:c.642+61G>A NP_002991.2:n.642+61G>A
NM_003000.3:c.642+61G>A MANE Select NP_002991.2:n.642+61G>A
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