HGVS | Genome Assembly |
---|---|
NC_000001.11:g.186680791T>A , CM000663.2:g.186680791T>A | GRCh38 |
NC_000001.10:g.186649923T>A , CM000663.1:g.186649923T>A | GRCh37 |
NC_000001.9:g.184916546T>A | NCBI36 |
NG_028206.2:g.4637A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000680451.1:c.-201A>T (PTGS2) | ENSP00000506242.1:n.-201A>T | |
NR_125801.1:n.138T>A (PACERR) |