Linked Data
MyVariant Identifiers:
chr3:g.169482667C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.169764879C>A , CM000665.2:g.169764879C>A | GRCh38 |
| NC_000003.11:g.169482667C>A , CM000665.1:g.169482667C>A | GRCh37 |
| NC_000003.10:g.170965361C>A | NCBI36 |
| NG_016363.1:g.5182G>T , LRG_347:g.5182G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_001566.1:n.182G>T , LRG_347t1:n.182G>T |