Linked Data
MyVariant Identifiers:
chr1:g.186649932A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186680800A>C , CM000663.2:g.186680800A>C | GRCh38 |
| NC_000001.10:g.186649932A>C , CM000663.1:g.186649932A>C | GRCh37 |
| NC_000001.9:g.184916555A>C | NCBI36 |
| NG_028206.2:g.4628T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000680451.1:c.-210T>G (PTGS2) | ENSP00000506242.1:n.-210T>G | |
| NR_125801.1:n.147A>C (PACERR) |