Canonical Allele Identifier: CA1156080174
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027799G= , CM000663.2:g.17027799G= GRCh38
NC_000001.10:g.17354294G= , CM000663.1:g.17354294G= GRCh37
NC_000001.9:g.17226881G= NCBI36
NG_012340.1:g.31372C= , LRG_316:g.31372C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.319C= ENSP00000481376.2:p.Gln107=
ENST00000491274.6:c.448C= ENSP00000480482.2:p.Gln150=
ENST00000375499.8:c.490C= MANE Select ENSP00000364649.3:p.Gln164=
ENST00000375499.7:c.490C= ENSP00000364649.3:p.Gln164=
ENST00000463045.2:c.319C= ENSP00000481376.1:p.Gln107=
ENST00000475506.1:n.407C=
ENST00000485515.5:n.424C=
ENST00000491274.5:c.448C= ENSP00000480482.1:p.Gln150=
NM_003000.2:c.490C= , LRG_316t1:c.490C= NP_002991.2:p.Gln164=
NM_003000.3:c.490C= MANE Select NP_002991.2:p.Gln164=