Linked Data
MyVariant Identifiers:
chr1:g.11907643G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11847586G>C , CM000663.2:g.11847586G>C | GRCh38 |
| NC_000001.10:g.11907643G>C , CM000663.1:g.11907643G>C | GRCh37 |
| NC_000001.9:g.11830230G>C | NCBI36 |
| NG_012926.1:g.5198C>G , LRG_751:g.5198C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000400892.3:c.*1971G>C (CLCN6) | ENSP00000496938.1:n.*1971G>C | |
| ENST00000446542.5:n.934G>C (NPPA-AS1) | ||
| ENST00000376476.1:c.-27-147C>G (NPPA) | ENSP00000365659.1:n.-27-147C>G | |
| ENST00000376480.7:c.99C>G (NPPA) MANE Select | ENSP00000365663.3:p.Ser33= | |
| ENST00000610706.1:c.99C>G (NPPA) | ENSP00000483195.1:p.Ser33= | |
| NM_006172.3:c.99C>G , LRG_751t1:c.99C>G (NPPA) | NP_006163.1:p.Ser33= | |
| NR_037806.1:n.1632G>C (NPPA-AS1) | ||
| NM_006172.4:c.99C>G (NPPA) MANE Select | NP_006163.1:p.Ser33= |