HGVS | Genome Assembly |
---|---|
NC_000001.11:g.186680799G>T , CM000663.2:g.186680799G>T | GRCh38 |
NC_000001.10:g.186649931G>T , CM000663.1:g.186649931G>T | GRCh37 |
NC_000001.9:g.184916554G>T | NCBI36 |
NG_028206.2:g.4629C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000680451.1:c.-209C>A (PTGS2) | ENSP00000506242.1:n.-209C>A | |
NR_125801.1:n.146G>T (PACERR) |