Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5046053T>A , CM000674.2:g.5046053T>A | GRCh38 |
| NC_000012.11:g.5155219T>A , CM000674.1:g.5155219T>A | GRCh37 |
| NC_000012.10:g.5025480T>A | NCBI36 |
| NG_012198.1:g.7135T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252321.5:c.*64T>A MANE Select | ENSP00000252321.3:n.*64T>A | |
| ENST00000252321.4:c.*64T>A | ENSP00000252321.3:n.*64T>A | |
| NM_002234.3:c.*64T>A | NP_002225.2:n.*64T>A | |
| NM_002234.4:c.*64T>A MANE Select | NP_002225.2:n.*64T>A |