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