Canonical Allele Identifier: CA1156077864
Gene: SDHB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022376C= , CM000663.2:g.17022376C= GRCh38
NC_000001.10:g.17348871C= , CM000663.1:g.17348871C= GRCh37
NC_000001.9:g.17221458C= NCBI36
NG_012340.1:g.36795G= , LRG_316:g.36795G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+232G= ENSP00000481376.2:n.594+232G=
ENST00000491274.6:c.723+232G= ENSP00000480482.2:n.723+232G=
ENST00000375499.8:c.765+232G= MANE Select ENSP00000364649.3:n.765+232G=
ENST00000375499.7:c.765+232G= ENSP00000364649.3:n.765+232G=
ENST00000475049.5:n.190+232G=
ENST00000485092.5:n.429+232G=
NM_003000.2:c.765+232G= , LRG_316t1:c.765+232G= NP_002991.2:n.765+232G=
NM_003000.3:c.765+232G= MANE Select NP_002991.2:n.765+232G=
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