Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.33850977A= , CM000682.2:g.33850977A= | GRCh38 |
| NC_000020.10:g.32438783A= , CM000682.1:g.32438783A= | GRCh37 |
| NC_000020.9:g.31902444A= | NCBI36 |
| NG_015820.1:g.44674A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000217402.3:c.394A= MANE Select | ENSP00000217402.2:p.Met132= | |
| ENST00000217402.2:c.394A= | ENSP00000217402.2:p.Met132= | |
| NM_176812.4:c.394A= | NP_789782.1:p.Met132= | |
| NM_176812.5:c.394A= MANE Select | NP_789782.1:p.Met132= |