Canonical Allele Identifier: CA1156080123
Gene: SDHB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027678C= , CM000663.2:g.17027678C= GRCh38
NC_000001.10:g.17354173C= , CM000663.1:g.17354173C= GRCh37
NC_000001.9:g.17226760C= NCBI36
NG_012340.1:g.31493G= , LRG_316:g.31493G=

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.369+71G= ENSP00000481376.2:n.369+71G=
ENST00000491274.6:c.498+71G= ENSP00000480482.2:n.498+71G=
ENST00000375499.8:c.540+71G= MANE Select ENSP00000364649.3:n.540+71G=
ENST00000375499.7:c.540+71G= ENSP00000364649.3:n.540+71G=
ENST00000475506.1:n.528G=
ENST00000485515.5:n.474+71G=
ENST00000491274.5:c.498+71G= ENSP00000480482.1:n.498+71G=
NM_003000.2:c.540+71G= , LRG_316t1:c.540+71G= NP_002991.2:n.540+71G=
NM_003000.3:c.540+71G= MANE Select NP_002991.2:n.540+71G=
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