Linked Data
gnomAD v4:
10-73249531-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.73249531T>C , CM000672.2:g.73249531T>C | GRCh38 |
| NC_000010.10:g.75009289T>C , CM000672.1:g.75009289T>C | GRCh37 |
| NC_000010.9:g.74679295T>C | NCBI36 |
| NG_008096.1:g.8163A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372945.8:c.*1321A>G (MRPS16) MANE Select | ENSP00000362036.3:n.*1321A>G | |
| ENST00000372940.3:c.275-213A>G (MRPS16) | ENSP00000362031.3:n.275-213A>G | |
| ENST00000372945.7:c.*1321A>G (MRPS16) | ENSP00000362036.3:n.*1321A>G | |
| ENST00000479005.1:n.1892A>G (MRPS16) | ||
| NM_016065.3:c.*1321A>G (MRPS16) | NP_057149.1:n.*1321A>G | |
| NR_038373.1:n.175+1081T>C (DNAJC9-AS1) | ||
| NM_016065.4:c.*1321A>G (MRPS16) MANE Select | NP_057149.1:n.*1321A>G |