Linked Data
ClinVar Variation Id:
1356806
ClinVar RCV Id:
RCV001870282
dbSNP Id:
rs2108182936
gnomAD v4:
3-169764763-C-T
MyVariant Identifiers:
chr3:g.169482551C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.169764763C>T , CM000665.2:g.169764763C>T | GRCh38 |
| NC_000003.11:g.169482551C>T , CM000665.1:g.169482551C>T | GRCh37 |
| NC_000003.10:g.170965245C>T | NCBI36 |
| NG_016363.1:g.5298G>A , LRG_347:g.5298G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_001566.1:n.298G>A , LRG_347t1:n.298G>A |