HGVS | Genome Assembly |
---|---|
NC_000001.11:g.186680812C>T , CM000663.2:g.186680812C>T | GRCh38 |
NC_000001.10:g.186649944C>T , CM000663.1:g.186649944C>T | GRCh37 |
NC_000001.9:g.184916567C>T | NCBI36 |
NG_028206.2:g.4616G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000680451.1:c.-222G>A (PTGS2) | ENSP00000506242.1:n.-222G>A | |
NR_125801.1:n.159C>T (PACERR) |