Canonical Allele Identifier: CA658655548
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17024014_17024020del , CM000663.2:g.17024014_17024020del GRCh38
NC_000001.10:g.17350509_17350515del , CM000663.1:g.17350509_17350515del GRCh37
NC_000001.9:g.17223096_17223102del NCBI36
NG_012340.1:g.35151_35157del , LRG_316:g.35151_35157del

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.424_430del ENSP00000481376.2:p.Tyr142GlyfsTer19
ENST00000491274.6:c.553_559del ENSP00000480482.2:p.Tyr185GlyfsTer19
ENST00000375499.8:c.595_601del MANE Select ENSP00000364649.3:p.Tyr199GlyfsTer19
ENST00000375499.7:c.595_601del ENSP00000364649.3:p.Tyr199GlyfsTer19
ENST00000485515.5:n.529_535del
ENST00000491274.5:c.553_559del ENSP00000480482.1:p.Tyr185GlyfsTer?
NM_003000.2:c.595_601del , LRG_316t1:c.595_601del NP_002991.2:p.Tyr199GlyfsTer19
NM_003000.3:c.595_601del MANE Select NP_002991.2:p.Tyr199GlyfsTer19