Annotation Detail

Information
Associated Genes
HBB LOC106099062 LOC107133510
Associated Variants
HBB p.Gln40Lys (p.Q40K) ( ENST00000485743.1, ENST00000335295.4, ENST00000647020.1 )
HBB p.Gln40Lys (p.Q40K) ( ENST00000335295.4, ENST00000485743.1, ENST00000647020.1 )
Source Database
ClinVar
Description
NM_000518.5(HBB):c.118C>A (p.Gln40Lys) AND HEMOGLOBIN ALABAMA
ClinVar Allele ID
799653
ClinVar RefSeq Alternation Syntax
NM_000518.5:c.118C>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/RCV002280786
Observed Origin Sample
germline
Pubmed
1115799
Drugs