Linked Data
dbSNP Id:
rs1392178327
MyVariant Identifiers:
chr1:g.186650039_186650040insAA (hg19)
chr1:g.186680907_186680908insAA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186680907_186680908insAA , CM000663.2:g.186680907_186680908insAA | GRCh38 |
| NC_000001.10:g.186650039_186650040insAA , CM000663.1:g.186650039_186650040insAA | GRCh37 |
| NC_000001.9:g.184916662_184916663insAA | NCBI36 |
| NG_028206.2:g.4520_4521insTT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000680451.1:c.-318_-317insTT (PTGS2) | ENSP00000506242.1:n.-318_-317insTT | |
| NR_125801.1:n.254_255insAA (PACERR) |