Canonical Allele Identifier: CA1156077799
Gene: SDHB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022213A= , CM000663.2:g.17022213A= GRCh38
NC_000001.10:g.17348708A= , CM000663.1:g.17348708A= GRCh37
NC_000001.9:g.17221295A= NCBI36
NG_012340.1:g.36958T= , LRG_316:g.36958T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+395T= ENSP00000481376.2:n.594+395T=
ENST00000491274.6:c.723+395T= ENSP00000480482.2:n.723+395T=
ENST00000375499.8:c.765+395T= MANE Select ENSP00000364649.3:n.765+395T=
ENST00000375499.7:c.765+395T= ENSP00000364649.3:n.765+395T=
ENST00000475049.5:n.190+395T=
ENST00000485092.5:n.429+395T=
NM_003000.2:c.765+395T= , LRG_316t1:c.765+395T= NP_002991.2:n.765+395T=
NM_003000.3:c.765+395T= MANE Select NP_002991.2:n.765+395T=
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