Linked Data
MyVariant Identifiers:
chr1:g.11904042T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11843985T>C , CM000663.2:g.11843985T>C | GRCh38 |
| NC_000001.10:g.11904042T>C , CM000663.1:g.11904042T>C | GRCh37 |
| NC_000001.9:g.11826629T>C | NCBI36 |
| NG_008766.1:g.42836T>C | |
| NG_012926.1:g.8799A>G , LRG_751:g.8799A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000400892.3:c.*1653T>C (CLCN6) | ENSP00000496938.1:n.*1653T>C | |
| ENST00000446542.5:n.473T>C (NPPA-AS1) | ||
| NR_037806.1:n.1171T>C (NPPA-AS1) |