Linked Data
ClinVar Variation Id:
1443750
ClinVar RCV Id:
RCV001981382
MyVariant Identifiers:
chr3:g.169482553G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.169764765G>T , CM000665.2:g.169764765G>T | GRCh38 |
| NC_000003.11:g.169482553G>T , CM000665.1:g.169482553G>T | GRCh37 |
| NC_000003.10:g.170965247G>T | NCBI36 |
| NG_016363.1:g.5296C>A , LRG_347:g.5296C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_001566.1:n.296C>A , LRG_347t1:n.296C>A |