Canonical Allele Identifier: CA1143492238
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028620C= , CM000663.2:g.17028620C= GRCh38
NC_000001.10:g.17355115C= , CM000663.1:g.17355115C= GRCh37
NC_000001.9:g.17227702C= NCBI36
NG_012340.1:g.30551G= , LRG_316:g.30551G=

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.232G= ENSP00000481376.2:p.Val78=
ENST00000491274.6:c.361G= ENSP00000480482.2:p.Val121=
ENST00000375499.8:c.403G= MANE Select ENSP00000364649.3:p.Val135=
ENST00000375499.7:c.403G= ENSP00000364649.3:p.Val135=
ENST00000463045.2:c.232G= ENSP00000481376.1:p.Val78=
ENST00000475506.1:n.320G=
ENST00000485515.5:n.357+34G=
ENST00000491274.5:c.361G= ENSP00000480482.1:p.Val121=
NM_003000.2:c.403G= , LRG_316t1:c.403G= NP_002991.2:p.Val135=
NM_003000.3:c.403G= MANE Select NP_002991.2:p.Val135=