Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.169764840C>T , CM000665.2:g.169764840C>T | GRCh38 |
| NC_000003.11:g.169482628C>T , CM000665.1:g.169482628C>T | GRCh37 |
| NC_000003.10:g.170965322C>T | NCBI36 |
| NG_016363.1:g.5221G>A , LRG_347:g.5221G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NR_001566.1:n.221G>A , LRG_347t1:n.221G>A |