Linked Data
ClinVar Variation Id:
952487
ClinVar RCV Id:
RCV001224606
dbSNP Id:
rs1303286129
MyVariant Identifiers:
chr3:g.169482683G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.169764895G>T , CM000665.2:g.169764895G>T | GRCh38 |
| NC_000003.11:g.169482683G>T , CM000665.1:g.169482683G>T | GRCh37 |
| NC_000003.10:g.170965377G>T | NCBI36 |
| NG_016363.1:g.5166C>A , LRG_347:g.5166C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_001566.1:n.166C>A , LRG_347t1:n.166C>A |