Canonical Allele Identifier: CA1140263947
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028667G= , CM000663.2:g.17028667G= GRCh38
NC_000001.10:g.17355162G= , CM000663.1:g.17355162G= GRCh37
NC_000001.9:g.17227749G= NCBI36
NG_012340.1:g.30504C= , LRG_316:g.30504C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.185C= ENSP00000481376.2:p.Thr62=
ENST00000491274.6:c.314C= ENSP00000480482.2:p.Thr105=
ENST00000375499.8:c.356C= MANE Select ENSP00000364649.3:p.Thr119=
ENST00000375499.7:c.356C= ENSP00000364649.3:p.Thr119=
ENST00000463045.2:c.185C= ENSP00000481376.1:p.Thr62=
ENST00000475506.1:n.273C=
ENST00000485515.5:n.344C=
ENST00000491274.5:c.314C= ENSP00000480482.1:p.Thr105=
NM_003000.2:c.356C= , LRG_316t1:c.356C= NP_002991.2:p.Thr119=
NM_003000.3:c.356C= MANE Select NP_002991.2:p.Thr119=