Annotation Detail

Information
Associated Genes
HBB LOC106099062 LOC107133510 LOC110006319
Associated Variants
HBB p.Glu122Gln (p.E122Q) ( ENST00000335295.4, ENST00000647020.1 )
HBB p.Ser10Tyr (p.S10Y) ( ENST00000647020.1, ENST00000485743.1, ENST00000335295.4 )
HBB p.Glu122Gln (p.E122Q) ( ENST00000335295.4, ENST00000647020.1 )
HBB p.Ser10Tyr (p.S10Y) ( ENST00000335295.4, ENST00000485743.1, ENST00000647020.1 )
Source Database
ClinVar
Description
NM_000518.4(HBB):c.[29C>A;364G>C] AND HEMOGLOBIN D (AGRI)
ClinVar Allele ID
30191
ClinVar Allele ID
30658
ClinVar RefSeq Alternation Syntax
NM_000518.5:c.364G>C
ClinVar RefSeq Alternation Syntax
NM_000518.5:c.29C>A
Clinical Significance Description
other
Clinical Significance Last Update
2017-12-12
Clinical Significance Review Status
no assertion criteria provided
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000016858
Observed Origin Sample
germline
Pubmed
11570725
Drugs