HGVS | Genome Assembly |
---|---|
NC_000001.11:g.186680839G>A , CM000663.2:g.186680839G>A | GRCh38 |
NC_000001.10:g.186649971G>A , CM000663.1:g.186649971G>A | GRCh37 |
NC_000001.9:g.184916594G>A | NCBI36 |
NG_028206.2:g.4589C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000680451.1:c.-249C>T (PTGS2) | ENSP00000506242.1:n.-249C>T | |
NR_125801.1:n.186G>A (PACERR) |