Canonical Allele Identifier: CA1143467676
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17044812T= , CM000663.2:g.17044812T= GRCh38
NC_000001.10:g.17371307T= , CM000663.1:g.17371307T= GRCh37
NC_000001.9:g.17243894T= NCBI36
NG_012340.1:g.14359A= , LRG_316:g.14359A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.-23A= ENSP00000481376.2:n.-23A=
ENST00000491274.6:c.107A= ENSP00000480482.2:p.Asp36=
ENST00000375499.8:c.149A= MANE Select ENSP00000364649.3:p.Asp50=
ENST00000375499.7:c.149A= ENSP00000364649.3:p.Asp50=
ENST00000463045.2:c.-23A= ENSP00000481376.1:n.-23A=
ENST00000466613.2:n.161A=
ENST00000475506.1:n.66A=
ENST00000485515.5:n.137A=
ENST00000491274.5:c.107A= ENSP00000480482.1:p.Asp36=
NM_003000.2:c.149A= , LRG_316t1:c.149A= NP_002991.2:p.Asp50=
NM_003000.3:c.149A= MANE Select NP_002991.2:p.Asp50=