Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7454424G>T , CM000679.2:g.7454424G>T | GRCh38 |
| NC_000017.10:g.7357743G>T , CM000679.1:g.7357743G>T | GRCh37 |
| NC_000017.9:g.7298467G>T | NCBI36 |
| NG_008026.1:g.14338G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306071.7:c.948G>T MANE Select | ENSP00000304290.2:p.Met316Ile | |
| ENST00000306071.6:c.948G>T | ENSP00000304290.2:p.Met316Ile | |
| ENST00000536404.6:c.732G>T | ENSP00000439209.2:p.Met244Ile | |
| ENST00000570557.5:c.611G>T | ||
| ENST00000573209.1:n.1892G>T | ||
| ENST00000576360.1:c.605-20G>T | ENSP00000459092.1:n.605-20G>T | |
| NM_000747.2:c.948G>T | NP_000738.2:p.Met316Ile | |
| NM_000747.3:c.948G>T MANE Select | NP_000738.2:p.Met316Ile |