Canonical Allele Identifier: CA1156080476
Gene: SDHB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028591G= , CM000663.2:g.17028591G= GRCh38
NC_000001.10:g.17355086G= , CM000663.1:g.17355086G= GRCh37
NC_000001.9:g.17227673G= NCBI36
NG_012340.1:g.30580C= , LRG_316:g.30580C=

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.252+9C= ENSP00000481376.2:n.252+9C=
ENST00000491274.6:c.381+9C= ENSP00000480482.2:n.381+9C=
ENST00000375499.8:c.423+9C= MANE Select ENSP00000364649.3:n.423+9C=
ENST00000375499.7:c.423+9C= ENSP00000364649.3:n.423+9C=
ENST00000463045.2:c.252+9C= ENSP00000481376.1:n.252+9C=
ENST00000475506.1:n.340+9C=
ENST00000485515.5:n.357+63C=
ENST00000491274.5:c.381+9C= ENSP00000480482.1:n.381+9C=
NM_003000.2:c.423+9C= , LRG_316t1:c.423+9C= NP_002991.2:n.423+9C=
NM_003000.3:c.423+9C= MANE Select NP_002991.2:n.423+9C=
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