Linked Data
MyVariant Identifiers:
chr1:g.186649958T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186680826T>G , CM000663.2:g.186680826T>G | GRCh38 |
| NC_000001.10:g.186649958T>G , CM000663.1:g.186649958T>G | GRCh37 |
| NC_000001.9:g.184916581T>G | NCBI36 |
| NG_028206.2:g.4602A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000680451.1:c.-236A>C (PTGS2) | ENSP00000506242.1:n.-236A>C | |
| NR_125801.1:n.173T>G (PACERR) |