Canonical Allele Identifier: CA1141648122
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027773C= , CM000663.2:g.17027773C= GRCh38
NC_000001.10:g.17354268C= , CM000663.1:g.17354268C= GRCh37
NC_000001.9:g.17226855C= NCBI36
NG_012340.1:g.31398G= , LRG_316:g.31398G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.345G= ENSP00000481376.2:p.Gln115=
ENST00000491274.6:c.474G= ENSP00000480482.2:p.Gln158=
ENST00000375499.8:c.516G= MANE Select ENSP00000364649.3:p.Gln172=
ENST00000375499.7:c.516G= ENSP00000364649.3:p.Gln172=
ENST00000463045.2:c.345G= ENSP00000481376.1:p.Gln115=
ENST00000475506.1:n.433G=
ENST00000485515.5:n.450G=
ENST00000491274.5:c.474G= ENSP00000480482.1:p.Gln158=
NM_003000.2:c.516G= , LRG_316t1:c.516G= NP_002991.2:p.Gln172=
NM_003000.3:c.516G= MANE Select NP_002991.2:p.Gln172=