Linked Data
dbSNP Id:
rs1665869847
gnomAD v4:
1-186680878-C-T
MyVariant Identifiers:
chr1:g.186650010C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186680878C>T , CM000663.2:g.186680878C>T | GRCh38 |
| NC_000001.10:g.186650010C>T , CM000663.1:g.186650010C>T | GRCh37 |
| NC_000001.9:g.184916633C>T | NCBI36 |
| NG_028206.2:g.4550G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000680451.1:c.-288G>A (PTGS2) | ENSP00000506242.1:n.-288G>A | |
| NR_125801.1:n.225C>T (PACERR) |