Linked Data
gnomAD v4:
10-73249400-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.73249400C>A , CM000672.2:g.73249400C>A | GRCh38 |
| NC_000010.10:g.75009158C>A , CM000672.1:g.75009158C>A | GRCh37 |
| NC_000010.9:g.74679164C>A | NCBI36 |
| NG_008096.1:g.8294G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372945.8:c.*1452G>T (MRPS16) MANE Select | ENSP00000362036.3:n.*1452G>T | |
| ENST00000372940.3:c.275-82G>T (MRPS16) | ENSP00000362031.3:n.275-82G>T | |
| ENST00000372945.7:c.*1452G>T (MRPS16) | ENSP00000362036.3:n.*1452G>T | |
| ENST00000479005.1:n.2023G>T (MRPS16) | ||
| NM_016065.3:c.*1452G>T (MRPS16) | NP_057149.1:n.*1452G>T | |
| NR_038373.1:n.175+950C>A (DNAJC9-AS1) | ||
| NM_016065.4:c.*1452G>T (MRPS16) MANE Select | NP_057149.1:n.*1452G>T |