Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.229431146A>G , CM000663.2:g.229431146A>G | GRCh38 |
| NC_000001.10:g.229566893A>G , CM000663.1:g.229566893A>G | GRCh37 |
| NC_000001.9:g.227633516A>G | NCBI36 |
| NG_006672.1:g.7951T>C , LRG_429:g.7951T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684723.1:c.*353T>C | ENSP00000508084.1:n.*353T>C |