Linked Data
ClinVar Variation Id:
1003718
ClinVar RCV Id:
RCV001300309
dbSNP Id:
rs1777963567
MyVariant Identifiers:
chr3:g.169482752A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.169764964A>C , CM000665.2:g.169764964A>C | GRCh38 |
| NC_000003.11:g.169482752A>C , CM000665.1:g.169482752A>C | GRCh37 |
| NC_000003.10:g.170965446A>C | NCBI36 |
| NG_016363.1:g.5097T>G , LRG_347:g.5097T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_001566.1:n.97T>G , LRG_347t1:n.97T>G |