HGVS | Genome Assembly |
---|---|
NC_000006.12:g.12290319T= , CM000668.2:g.12290319T= | GRCh38 |
NC_000006.11:g.12290552T= , CM000668.1:g.12290552T= | GRCh37 |
NC_000006.10:g.12398538T= | NCBI36 |
NG_016196.1:g.5024T= |
HGVS | Amino-acid Change | |
---|---|---|
NM_001168319.1:c.-311T= | NP_001161791.1:n.-311T= | |
NM_001955.4:c.-311T= | NP_001946.3:n.-311T= | |
XM_011514330.1:c.-1-310T= | XP_011512632.1:n.-1-310T= | |
XM_011514331.1:c.-1-310T= | XP_011512633.1:n.-1-310T= | |
XM_011514332.1:c.-1-310T= | XP_011512634.1:n.-1-310T= | |
XM_011514330.2:c.-1-310T= | XP_011512632.1:n.-1-310T= | |
XM_011514331.3:c.-1-310T= | XP_011512633.1:n.-1-310T= | |
XM_011514332.2:c.-1-310T= | XP_011512634.1:n.-1-310T= | |
XM_017010331.1:c.-2+196T= | XP_016865820.1:n.-2+196T= |