HGVS | Genome Assembly |
---|---|
NC_000006.12:g.12290274T>C , CM000668.2:g.12290274T>C | GRCh38 |
NC_000006.11:g.12290507T>C , CM000668.1:g.12290507T>C | GRCh37 |
NC_000006.10:g.12398493T>C | NCBI36 |
NG_016196.1:g.4979T>C |
HGVS | Amino-acid Change | |
---|---|---|
XM_011514330.1:c.-1-355T>C | XP_011512632.1:n.-1-355T>C | |
XM_011514331.1:c.-1-355T>C | XP_011512633.1:n.-1-355T>C | |
XM_011514332.1:c.-1-355T>C | XP_011512634.1:n.-1-355T>C | |
XM_011514330.2:c.-1-355T>C | XP_011512632.1:n.-1-355T>C | |
XM_011514331.3:c.-1-355T>C | XP_011512633.1:n.-1-355T>C | |
XM_011514332.2:c.-1-355T>C | XP_011512634.1:n.-1-355T>C | |
XM_017010331.1:c.-2+151T>C | XP_016865820.1:n.-2+151T>C |