Canonical Allele Identifier: CA1156077802
Gene: SDHB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022221G= , CM000663.2:g.17022221G= GRCh38
NC_000001.10:g.17348716G= , CM000663.1:g.17348716G= GRCh37
NC_000001.9:g.17221303G= NCBI36
NG_012340.1:g.36950C= , LRG_316:g.36950C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+387C= ENSP00000481376.2:n.594+387C=
ENST00000491274.6:c.723+387C= ENSP00000480482.2:n.723+387C=
ENST00000375499.8:c.765+387C= MANE Select ENSP00000364649.3:n.765+387C=
ENST00000375499.7:c.765+387C= ENSP00000364649.3:n.765+387C=
ENST00000475049.5:n.190+387C=
ENST00000485092.5:n.429+387C=
NM_003000.2:c.765+387C= , LRG_316t1:c.765+387C= NP_002991.2:n.765+387C=
NM_003000.3:c.765+387C= MANE Select NP_002991.2:n.765+387C=
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