Canonical Allele Identifier: CA1156080169
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027787G= , CM000663.2:g.17027787G= GRCh38
NC_000001.10:g.17354282G= , CM000663.1:g.17354282G= GRCh37
NC_000001.9:g.17226869G= NCBI36
NG_012340.1:g.31384C= , LRG_316:g.31384C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.331C= ENSP00000481376.2:p.Gln111=
ENST00000491274.6:c.460C= ENSP00000480482.2:p.Gln154=
ENST00000375499.8:c.502C= MANE Select ENSP00000364649.3:p.Gln168=
ENST00000375499.7:c.502C= ENSP00000364649.3:p.Gln168=
ENST00000463045.2:c.331C= ENSP00000481376.1:p.Gln111=
ENST00000475506.1:n.419C=
ENST00000485515.5:n.436C=
ENST00000491274.5:c.460C= ENSP00000480482.1:p.Gln154=
NM_003000.2:c.502C= , LRG_316t1:c.502C= NP_002991.2:p.Gln168=
NM_003000.3:c.502C= MANE Select NP_002991.2:p.Gln168=