Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94007623A= , CM000663.2:g.94007623A= | GRCh38 |
| NC_000001.10:g.94473179A= , CM000663.1:g.94473179A= | GRCh37 |
| NC_000001.9:g.94245767A= | NCBI36 |
| NG_009073.1:g.118527T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.6005+11T= MANE Select | ENSP00000359245.3:n.6005+11T= | |
| ENST00000370225.3:c.6005+11T= | ENSP00000359245.3:n.6005+11T= | |
| ENST00000465352.1:n.421+11T= | ||
| ENST00000484388.1:n.119+11T= | ||
| ENST00000536513.5:c.2381+11T= | ENSP00000439707.2:n.2381+11T= | |
| NM_000350.2:c.6005+11T= | NP_000341.2:n.6005+11T= | |
| NM_000350.3:c.6005+11T= MANE Select | NP_000341.2:n.6005+11T= |