Canonical Allele Identifier: CA1156080485
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028617T= , CM000663.2:g.17028617T= GRCh38
NC_000001.10:g.17355112T= , CM000663.1:g.17355112T= GRCh37
NC_000001.9:g.17227699T= NCBI36
NG_012340.1:g.30554A= , LRG_316:g.30554A=

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.235A= ENSP00000481376.2:p.Ile79=
ENST00000491274.6:c.364A= ENSP00000480482.2:p.Ile122=
ENST00000375499.8:c.406A= MANE Select ENSP00000364649.3:p.Ile136=
ENST00000375499.7:c.406A= ENSP00000364649.3:p.Ile136=
ENST00000463045.2:c.235A= ENSP00000481376.1:p.Ile79=
ENST00000475506.1:n.323A=
ENST00000485515.5:n.357+37A=
ENST00000491274.5:c.364A= ENSP00000480482.1:p.Ile122=
NM_003000.2:c.406A= , LRG_316t1:c.406A= NP_002991.2:p.Ile136=
NM_003000.3:c.406A= MANE Select NP_002991.2:p.Ile136=