HGVS | Genome Assembly |
---|---|
NC_000001.11:g.186680866A>G , CM000663.2:g.186680866A>G | GRCh38 |
NC_000001.10:g.186649998A>G , CM000663.1:g.186649998A>G | GRCh37 |
NC_000001.9:g.184916621A>G | NCBI36 |
NG_028206.2:g.4562T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000680451.1:c.-276T>C (PTGS2) | ENSP00000506242.1:n.-276T>C | |
NR_125801.1:n.213A>G (PACERR) |