Linked Data
MyVariant Identifiers:
chr1:g.186649954C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186680822C>G , CM000663.2:g.186680822C>G | GRCh38 |
| NC_000001.10:g.186649954C>G , CM000663.1:g.186649954C>G | GRCh37 |
| NC_000001.9:g.184916577C>G | NCBI36 |
| NG_028206.2:g.4606G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000680451.1:c.-232G>C (PTGS2) | ENSP00000506242.1:n.-232G>C | |
| NR_125801.1:n.169C>G (PACERR) |