Linked Data
MyVariant Identifiers:
chr1:g.11903982T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11843925T>G , CM000663.2:g.11843925T>G | GRCh38 |
| NC_000001.10:g.11903982T>G , CM000663.1:g.11903982T>G | GRCh37 |
| NC_000001.9:g.11826569T>G | NCBI36 |
| NG_008766.1:g.42776T>G | |
| NG_012926.1:g.8859A>C , LRG_751:g.8859A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000400892.3:c.*1593T>G (CLCN6) | ENSP00000496938.1:n.*1593T>G | |
| ENST00000446542.5:n.413T>G (NPPA-AS1) | ||
| NR_037806.1:n.1111T>G (NPPA-AS1) |