Linked Data
MyVariant Identifiers:
chr1:g.186649967C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186680835C>A , CM000663.2:g.186680835C>A | GRCh38 |
| NC_000001.10:g.186649967C>A , CM000663.1:g.186649967C>A | GRCh37 |
| NC_000001.9:g.184916590C>A | NCBI36 |
| NG_028206.2:g.4593G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000680451.1:c.-245G>T (PTGS2) | ENSP00000506242.1:n.-245G>T | |
| NR_125801.1:n.182C>A (PACERR) |