Canonical Allele Identifier: CA2742638187
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028356_17028359del , CM000663.2:g.17028356_17028359del GRCh38
NC_000001.10:g.17354851_17354854del , CM000663.1:g.17354851_17354854del GRCh37
NC_000001.9:g.17227438_17227441del NCBI36
NG_012340.1:g.30814_30817del , LRG_316:g.30814_30817del

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.252+243_252+246del ENSP00000481376.2:n.252+243_252+246del
ENST00000491274.6:c.381+243_381+246del ENSP00000480482.2:n.381+243_381+246del
ENST00000375499.8:c.423+243_423+246del MANE Select ENSP00000364649.3:n.423+243_423+246del
ENST00000375499.7:c.423+243_423+246del ENSP00000364649.3:n.423+243_423+246del
ENST00000463045.2:c.252+243_252+246del ENSP00000481376.1:n.252+243_252+246del
ENST00000475506.1:n.340+243_340+246del
ENST00000485515.5:n.357+297_357+300del
ENST00000491274.5:c.381+243_381+246del ENSP00000480482.1:n.381+243_381+246del
NM_003000.2:c.423+243_423+246del , LRG_316t1:c.423+243_423+246del NP_002991.2:n.423+243_423+246del
NM_003000.3:c.423+243_423+246del MANE Select NP_002991.2:n.423+243_423+246del