Linked Data
MyVariant Identifiers:
chr1:g.186649983T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186680851T>C , CM000663.2:g.186680851T>C | GRCh38 |
| NC_000001.10:g.186649983T>C , CM000663.1:g.186649983T>C | GRCh37 |
| NC_000001.9:g.184916606T>C | NCBI36 |
| NG_028206.2:g.4577A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000680451.1:c.-261A>G (PTGS2) | ENSP00000506242.1:n.-261A>G | |
| NR_125801.1:n.198T>C (PACERR) |