Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87727305T= , CM000672.2:g.87727305T= | GRCh38 |
| NC_000010.10:g.89487062T= , CM000672.1:g.89487062T= | GRCh37 |
| NC_000010.9:g.89477042T= | NCBI36 |
| NG_012150.1:g.72587T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000456849.2:c.902T= MANE Select | ENSP00000406157.1:p.Ile301= | |
| ENST00000361175.8:c.887T= | ENSP00000354436.4:p.Ile296= | |
| ENST00000456849.1:c.902T= | ENSP00000406157.1:p.Ile301= | |
| NM_001015880.1:c.902T= | NP_001015880.1:p.Ile301= | |
| NM_004670.3:c.887T= | NP_004661.2:p.Ile296= | |
| NM_001015880.2:c.902T= MANE Select | NP_001015880.1:p.Ile301= | |
| NM_004670.4:c.887T= | NP_004661.2:p.Ile296= |