Linked Data
MyVariant Identifiers:
chr1:g.186650000T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186680868T>G , CM000663.2:g.186680868T>G | GRCh38 |
| NC_000001.10:g.186650000T>G , CM000663.1:g.186650000T>G | GRCh37 |
| NC_000001.9:g.184916623T>G | NCBI36 |
| NG_028206.2:g.4560A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000680451.1:c.-278A>C (PTGS2) | ENSP00000506242.1:n.-278A>C | |
| NR_125801.1:n.215T>G (PACERR) |