Canonical Allele Identifier: CA1156080490
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028638G= , CM000663.2:g.17028638G= GRCh38
NC_000001.10:g.17355133G= , CM000663.1:g.17355133G= GRCh37
NC_000001.9:g.17227720G= NCBI36
NG_012340.1:g.30533C= , LRG_316:g.30533C=

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.214C= ENSP00000481376.2:p.Pro72=
ENST00000491274.6:c.343C= ENSP00000480482.2:p.Pro115=
ENST00000375499.8:c.385C= MANE Select ENSP00000364649.3:p.Pro129=
ENST00000375499.7:c.385C= ENSP00000364649.3:p.Pro129=
ENST00000463045.2:c.214C= ENSP00000481376.1:p.Pro72=
ENST00000475506.1:n.302C=
ENST00000485515.5:n.357+16C=
ENST00000491274.5:c.343C= ENSP00000480482.1:p.Pro115=
NM_003000.2:c.385C= , LRG_316t1:c.385C= NP_002991.2:p.Pro129=
NM_003000.3:c.385C= MANE Select NP_002991.2:p.Pro129=