Canonical Allele Identifier: CA1156078011
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022694T= , CM000663.2:g.17022694T= GRCh38
NC_000001.10:g.17349189T= , CM000663.1:g.17349189T= GRCh37
NC_000001.9:g.17221776T= NCBI36
NG_012340.1:g.36477A= , LRG_316:g.36477A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.508A= ENSP00000481376.2:p.Thr170=
ENST00000491274.6:c.637A= ENSP00000480482.2:p.Thr213=
ENST00000375499.8:c.679A= MANE Select ENSP00000364649.3:p.Thr227=
ENST00000375499.7:c.679A= ENSP00000364649.3:p.Thr227=
ENST00000475049.5:n.104A=
ENST00000485092.5:n.343A=
ENST00000485515.5:n.613A=
NM_003000.2:c.679A= , LRG_316t1:c.679A= NP_002991.2:p.Thr227=
NM_003000.3:c.679A= MANE Select NP_002991.2:p.Thr227=