Linked Data
ClinVar Variation Id:
2146368
ClinVar RCV Id:
RCV003067095
dbSNP Id:
rs1777965400
MyVariant Identifiers:
chr3:g.169482823C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.169765035C>A , CM000665.2:g.169765035C>A | GRCh38 |
| NC_000003.11:g.169482823C>A , CM000665.1:g.169482823C>A | GRCh37 |
| NC_000003.10:g.170965517C>A | NCBI36 |
| NG_016363.1:g.5026G>T , LRG_347:g.5026G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_001566.1:n.26G>T , LRG_347t1:n.26G>T |