HGVS | Genome Assembly |
---|---|
NC_000001.11:g.186680825C>A , CM000663.2:g.186680825C>A | GRCh38 |
NC_000001.10:g.186649957C>A , CM000663.1:g.186649957C>A | GRCh37 |
NC_000001.9:g.184916580C>A | NCBI36 |
NG_028206.2:g.4603G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000680451.1:c.-235G>T (PTGS2) | ENSP00000506242.1:n.-235G>T | |
NR_125801.1:n.172C>A (PACERR) |