Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10673757A= , CM000682.2:g.10673757A= | GRCh38 |
| NC_000020.10:g.10654405A= , CM000682.1:g.10654405A= | GRCh37 |
| NC_000020.9:g.10602405A= | NCBI36 |
| NG_007496.1:g.5290T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.-227T= MANE Select | ENSP00000254958.4:n.-227T= | |
| ENST00000254958.9:c.-227T= | ENSP00000254958.4:n.-227T= | |
| NM_000214.2:c.-227T= | NP_000205.1:n.-227T= | |
| NM_000214.3:c.-227T= MANE Select | NP_000205.1:n.-227T= |