Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.119320671C>A , CM000666.2:g.119320671C>A | GRCh38 |
| NC_000004.11:g.120241826C>A , CM000666.1:g.120241826C>A | GRCh37 |
| NC_000004.10:g.120461274C>A | NCBI36 |
| NG_011444.1:g.6491G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000274024.4:c.239G>T MANE Select | ENSP00000274024.3:p.Arg80Met | |
| ENST00000274024.3:c.239G>T | ENSP00000274024.3:p.Arg80Met | |
| NM_000134.3:c.239G>T | NP_000125.2:p.Arg80Met | |
| NM_000134.4:c.239G>T MANE Select | NP_000125.2:p.Arg80Met |