Linked Data
MyVariant Identifiers:
chr1:g.186649992G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186680860G>C , CM000663.2:g.186680860G>C | GRCh38 |
| NC_000001.10:g.186649992G>C , CM000663.1:g.186649992G>C | GRCh37 |
| NC_000001.9:g.184916615G>C | NCBI36 |
| NG_028206.2:g.4568C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000680451.1:c.-270C>G (PTGS2) | ENSP00000506242.1:n.-270C>G | |
| NR_125801.1:n.207G>C (PACERR) |