Linked Data
ClinVar Variation Id:
1693878
ClinVar RCV Id:
RCV002261747
dbSNP Id:
rs2108183154
MyVariant Identifiers:
chr3:g.169482677T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.169764889T>C , CM000665.2:g.169764889T>C | GRCh38 |
| NC_000003.11:g.169482677T>C , CM000665.1:g.169482677T>C | GRCh37 |
| NC_000003.10:g.170965371T>C | NCBI36 |
| NG_016363.1:g.5172A>G , LRG_347:g.5172A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_001566.1:n.172A>G , LRG_347t1:n.172A>G |