Canonical Allele Identifier: CA1148402004
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027765T= , CM000663.2:g.17027765T= GRCh38
NC_000001.10:g.17354260T= , CM000663.1:g.17354260T= GRCh37
NC_000001.9:g.17226847T= NCBI36
NG_012340.1:g.31406A= , LRG_316:g.31406A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.353A= ENSP00000481376.2:p.Glu118=
ENST00000491274.6:c.482A= ENSP00000480482.2:p.Glu161=
ENST00000375499.8:c.524A= MANE Select ENSP00000364649.3:p.Glu175=
ENST00000375499.7:c.524A= ENSP00000364649.3:p.Glu175=
ENST00000463045.2:c.353A= ENSP00000481376.1:p.Glu118=
ENST00000475506.1:n.441A=
ENST00000485515.5:n.458A=
ENST00000491274.5:c.482A= ENSP00000480482.1:p.Glu161=
NM_003000.2:c.524A= , LRG_316t1:c.524A= NP_002991.2:p.Glu175=
NM_003000.3:c.524A= MANE Select NP_002991.2:p.Glu175=