Linked Data
dbSNP Id:
rs987964927
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11847183C>G , CM000663.2:g.11847183C>G | GRCh38 |
| NC_000001.10:g.11907240C>G , CM000663.1:g.11907240C>G | GRCh37 |
| NC_000001.9:g.11829827C>G | NCBI36 |
| NG_012926.1:g.5601G>C , LRG_751:g.5601G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000400892.3:c.*1962-394C>G (CLCN6) | ENSP00000496938.1:n.*1962-394C>G | |
| ENST00000446542.5:n.782-251C>G (NPPA-AS1) | ||
| ENST00000376476.1:c.230G>C (NPPA) | ENSP00000365659.1:p.Arg77Thr | |
| ENST00000376480.7:c.380G>C (NPPA) MANE Select | ENSP00000365663.3:p.Arg127Thr | |
| ENST00000610706.1:c.380G>C (NPPA) | ENSP00000483195.1:p.Arg127Thr | |
| NM_006172.3:c.380G>C , LRG_751t1:c.380G>C (NPPA) | NP_006163.1:p.Arg127Thr | |
| NR_037806.1:n.1480-251C>G (NPPA-AS1) | ||
| NM_006172.4:c.380G>C (NPPA) MANE Select | NP_006163.1:p.Arg127Thr |