Linked Data
ClinVar Variation Id:
933281
ClinVar RCV Id:
RCV001201459
dbSNP Id:
rs1777962078
MyVariant Identifiers:
chr3:g.169482667C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.169764879C>G , CM000665.2:g.169764879C>G | GRCh38 |
| NC_000003.11:g.169482667C>G , CM000665.1:g.169482667C>G | GRCh37 |
| NC_000003.10:g.170965361C>G | NCBI36 |
| NG_016363.1:g.5182G>C , LRG_347:g.5182G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_001566.1:n.182G>C , LRG_347t1:n.182G>C |