HGVS | Genome Assembly |
---|---|
NC_000012.12:g.53500681G>C , CM000674.2:g.53500681G>C | GRCh38 |
NC_000012.11:g.53894465G>C , CM000674.1:g.53894465G>C | GRCh37 |
NC_000012.10:g.52180732G>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XM_005269120.3:c.-1143G>C (TARBP2) | XP_005269177.1:n.-1143G>C | |
XM_011538725.3:c.-691C>G (MAP3K12) | XP_011537027.1:n.-691C>G |