Linked Data
MyVariant Identifiers:
chr1:g.11903980C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11843923C>A , CM000663.2:g.11843923C>A | GRCh38 |
| NC_000001.10:g.11903980C>A , CM000663.1:g.11903980C>A | GRCh37 |
| NC_000001.9:g.11826567C>A | NCBI36 |
| NG_008766.1:g.42774C>A | |
| NG_012926.1:g.8861G>T , LRG_751:g.8861G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000400892.3:c.*1591C>A (CLCN6) | ENSP00000496938.1:n.*1591C>A | |
| ENST00000446542.5:n.411C>A (NPPA-AS1) | ||
| NR_037806.1:n.1109C>A (NPPA-AS1) |