Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52814255T>C , CM000674.2:g.52814255T>C | GRCh38 |
| NC_000012.11:g.53208039T>C , CM000674.1:g.53208039T>C | GRCh37 |
| NC_000012.10:g.51494306T>C | NCBI36 |
| NG_007380.1:g.5297A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000551956.1:c.-197A>G | ENSP00000448220.1:n.-197A>G |