Canonical Allele Identifier: CA1156080438
Gene: SDHB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028475T= , CM000663.2:g.17028475T= GRCh38
NC_000001.10:g.17354970T= , CM000663.1:g.17354970T= GRCh37
NC_000001.9:g.17227557T= NCBI36
NG_012340.1:g.30696A= , LRG_316:g.30696A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.252+125A= ENSP00000481376.2:n.252+125A=
ENST00000491274.6:c.381+125A= ENSP00000480482.2:n.381+125A=
ENST00000375499.8:c.423+125A= MANE Select ENSP00000364649.3:n.423+125A=
ENST00000375499.7:c.423+125A= ENSP00000364649.3:n.423+125A=
ENST00000463045.2:c.252+125A= ENSP00000481376.1:n.252+125A=
ENST00000475506.1:n.340+125A=
ENST00000485515.5:n.357+179A=
ENST00000491274.5:c.381+125A= ENSP00000480482.1:n.381+125A=
NM_003000.2:c.423+125A= , LRG_316t1:c.423+125A= NP_002991.2:n.423+125A=
NM_003000.3:c.423+125A= MANE Select NP_002991.2:n.423+125A=
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