Linked Data
dbSNP Id:
rs1302076118
gnomAD v3:
1-186680852-C-T
gnomAD v4:
1-186680852-C-T
MyVariant Identifiers:
chr1:g.186649984C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186680852C>T , CM000663.2:g.186680852C>T | GRCh38 |
| NC_000001.10:g.186649984C>T , CM000663.1:g.186649984C>T | GRCh37 |
| NC_000001.9:g.184916607C>T | NCBI36 |
| NG_028206.2:g.4576G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000680451.1:c.-262G>A (PTGS2) | ENSP00000506242.1:n.-262G>A | |
| NR_125801.1:n.199C>T (PACERR) |