HGVS | Genome Assembly |
---|---|
NC_000006.12:g.12290351T>C , CM000668.2:g.12290351T>C | GRCh38 |
NC_000006.11:g.12290584T>C , CM000668.1:g.12290584T>C | GRCh37 |
NC_000006.10:g.12398570T>C | NCBI36 |
NG_016196.1:g.5056T>C |
HGVS | Amino-acid Change | |
---|---|---|
NM_001168319.1:c.-279T>C | NP_001161791.1:n.-279T>C | |
NM_001955.4:c.-279T>C | NP_001946.3:n.-279T>C | |
XM_011514330.1:c.-1-278T>C | XP_011512632.1:n.-1-278T>C | |
XM_011514331.1:c.-1-278T>C | XP_011512633.1:n.-1-278T>C | |
XM_011514332.1:c.-1-278T>C | XP_011512634.1:n.-1-278T>C | |
XM_011514330.2:c.-1-278T>C | XP_011512632.1:n.-1-278T>C | |
XM_011514331.3:c.-1-278T>C | XP_011512633.1:n.-1-278T>C | |
XM_011514332.2:c.-1-278T>C | XP_011512634.1:n.-1-278T>C | |
XM_017010331.1:c.-2+228T>C | XP_016865820.1:n.-2+228T>C |