Linked Data
MyVariant Identifiers:
chr1:g.186650001C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186680869C>G , CM000663.2:g.186680869C>G | GRCh38 |
| NC_000001.10:g.186650001C>G , CM000663.1:g.186650001C>G | GRCh37 |
| NC_000001.9:g.184916624C>G | NCBI36 |
| NG_028206.2:g.4559G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000680451.1:c.-279G>C (PTGS2) | ENSP00000506242.1:n.-279G>C | |
| NR_125801.1:n.216C>G (PACERR) |