Linked Data
MyVariant Identifiers:
chr1:g.11907673G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11847616G>C , CM000663.2:g.11847616G>C | GRCh38 |
| NC_000001.10:g.11907673G>C , CM000663.1:g.11907673G>C | GRCh37 |
| NC_000001.9:g.11830260G>C | NCBI36 |
| NG_012926.1:g.5168C>G , LRG_751:g.5168C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000400892.3:c.*2001G>C (CLCN6) | ENSP00000496938.1:n.*2001G>C | |
| ENST00000446542.5:n.964G>C (NPPA-AS1) | ||
| ENST00000376476.1:c.-27-177C>G (NPPA) | ENSP00000365659.1:n.-27-177C>G | |
| ENST00000376480.7:c.69C>G (NPPA) MANE Select | ENSP00000365663.3:p.Thr23= | |
| ENST00000610706.1:c.69C>G (NPPA) | ENSP00000483195.1:p.Thr23= | |
| NM_006172.3:c.69C>G , LRG_751t1:c.69C>G (NPPA) | NP_006163.1:p.Thr23= | |
| NR_037806.1:n.1662G>C (NPPA-AS1) | ||
| NM_006172.4:c.69C>G (NPPA) MANE Select | NP_006163.1:p.Thr23= |