Linked Data
MyVariant Identifiers:
chr1:g.11904118C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11844061C>G , CM000663.2:g.11844061C>G | GRCh38 |
| NC_000001.10:g.11904118C>G , CM000663.1:g.11904118C>G | GRCh37 |
| NC_000001.9:g.11826705C>G | NCBI36 |
| NG_008766.1:g.42912C>G | |
| NG_012926.1:g.8723G>C , LRG_751:g.8723G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000400892.3:c.*1729C>G (CLCN6) | ENSP00000496938.1:n.*1729C>G | |
| ENST00000446542.5:n.549C>G (NPPA-AS1) | ||
| NR_037806.1:n.1247C>G (NPPA-AS1) |