Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5233028A>T , CM000673.2:g.5233028A>T | GRCh38 |
| NC_000011.9:g.5254258A>T , CM000673.1:g.5254258A>T | GRCh37 |
| NC_000011.8:g.5210834A>T | NCBI36 |
| NG_000007.3:g.64588T>A | |
| NG_063112.2:g.15630T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000643122.1:c.380T>A | ENSP00000494708.1:p.Met127Lys | |
| ENST00000650601.1:c.380T>A MANE Select | ENSP00000497529.1:p.Met127Lys | |
| ENST00000292901.7:c.316-230T>A | ENSP00000292901.3:n.316-230T>A | |
| ENST00000380299.3:c.380T>A | ENSP00000369654.3:p.Met127Lys | |
| ENST00000417377.1:c.157T>A | ENSP00000414741.1:p.Cys53Ser | |
| NM_000519.3:c.380T>A | NP_000510.1:p.Met127Lys | |
| NM_000519.4:c.380T>A MANE Select | NP_000510.1:p.Met127Lys |