Linked Data
ClinVar Variation Id:
2099633
ClinVar RCV Id:
RCV003023103
MyVariant Identifiers:
chr3:g.169482806A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.169765018A>G , CM000665.2:g.169765018A>G | GRCh38 |
| NC_000003.11:g.169482806A>G , CM000665.1:g.169482806A>G | GRCh37 |
| NC_000003.10:g.170965500A>G | NCBI36 |
| NG_016363.1:g.5043T>C , LRG_347:g.5043T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_001566.1:n.43T>C , LRG_347t1:n.43T>C |