Linked Data
MyVariant Identifiers:
chr10:g.75011741G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.73251983G>T , CM000672.2:g.73251983G>T | GRCh38 |
| NC_000010.10:g.75011741G>T , CM000672.1:g.75011741G>T | GRCh37 |
| NC_000010.9:g.74681747G>T | NCBI36 |
| NG_008096.1:g.5711C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372945.8:c.54C>A (MRPS16) MANE Select | ENSP00000362036.3:p.Thr18= | |
| ENST00000372940.3:c.54C>A (MRPS16) | ENSP00000362031.3:p.Thr18= | |
| ENST00000372945.7:c.54C>A (MRPS16) | ENSP00000362036.3:p.Thr18= | |
| ENST00000471251.5:n.187C>A (MRPS16) | ||
| ENST00000473427.1:n.144C>A (MRPS16) | ||
| ENST00000479005.1:n.211C>A (MRPS16) | ||
| NM_016065.3:c.54C>A (MRPS16) | NP_057149.1:p.Thr18= | |
| NR_038373.1:n.175+3533G>T (DNAJC9-AS1) | ||
| XR_946059.1:n.120+242G>T | ||
| NM_016065.4:c.54C>A (MRPS16) MANE Select | NP_057149.1:p.Thr18= |