Linked Data
ClinVar Variation Id:
1441792
ClinVar RCV Id:
RCV001968013
dbSNP Id:
rs1336050074
MyVariant Identifiers:
chr3:g.169482820A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.169765032A>G , CM000665.2:g.169765032A>G | GRCh38 |
| NC_000003.11:g.169482820A>G , CM000665.1:g.169482820A>G | GRCh37 |
| NC_000003.10:g.170965514A>G | NCBI36 |
| NG_016363.1:g.5029T>C , LRG_347:g.5029T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_001566.1:n.29T>C , LRG_347t1:n.29T>C |