Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.73251801C>T , CM000672.2:g.73251801C>T | GRCh38 |
| NC_000010.10:g.75011559C>T , CM000672.1:g.75011559C>T | GRCh37 |
| NC_000010.9:g.74681565C>T | NCBI36 |
| NG_008096.1:g.5893G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372945.8:c.236G>A (MRPS16) MANE Select | ENSP00000362036.3:p.Cys79Tyr | |
| ENST00000372940.3:c.236G>A (MRPS16) | ENSP00000362031.3:p.Cys79Tyr | |
| ENST00000372945.7:c.236G>A (MRPS16) | ENSP00000362036.3:p.Cys79Tyr | |
| ENST00000471251.5:n.369G>A (MRPS16) | ||
| ENST00000473427.1:n.326G>A (MRPS16) | ||
| ENST00000479005.1:n.393G>A (MRPS16) | ||
| NM_016065.3:c.236G>A (MRPS16) | NP_057149.1:p.Cys79Tyr | |
| NR_038373.1:n.175+3351C>T (DNAJC9-AS1) | ||
| XR_946059.1:n.120+60C>T | ||
| NM_016065.4:c.236G>A (MRPS16) MANE Select | NP_057149.1:p.Cys79Tyr |