Canonical Allele Identifier: CA1156080202
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027849T= , CM000663.2:g.17027849T= GRCh38
NC_000001.10:g.17354344T= , CM000663.1:g.17354344T= GRCh37
NC_000001.9:g.17226931T= NCBI36
NG_012340.1:g.31322A= , LRG_316:g.31322A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.269A= ENSP00000481376.2:p.Tyr90=
ENST00000491274.6:c.398A= ENSP00000480482.2:p.Tyr133=
ENST00000375499.8:c.440A= MANE Select ENSP00000364649.3:p.Tyr147=
ENST00000375499.7:c.440A= ENSP00000364649.3:p.Tyr147=
ENST00000463045.2:c.269A= ENSP00000481376.1:p.Tyr90=
ENST00000475506.1:n.357A=
ENST00000485515.5:n.374A=
ENST00000491274.5:c.398A= ENSP00000480482.1:p.Tyr133=
NM_003000.2:c.440A= , LRG_316t1:c.440A= NP_002991.2:p.Tyr147=
NM_003000.3:c.440A= MANE Select NP_002991.2:p.Tyr147=