Linked Data
ClinVar Variation Id:
1005898
ClinVar RCV Id:
RCV001302849
dbSNP Id:
rs1553915617
MyVariant Identifiers:
chr3:g.169482742C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.169764954C>G , CM000665.2:g.169764954C>G | GRCh38 |
| NC_000003.11:g.169482742C>G , CM000665.1:g.169482742C>G | GRCh37 |
| NC_000003.10:g.170965436C>G | NCBI36 |
| NG_016363.1:g.5107G>C , LRG_347:g.5107G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_001566.1:n.107G>C , LRG_347t1:n.107G>C |