HGVS | Genome Assembly |
---|---|
NC_000023.11:g.68829660G= , CM000685.2:g.68829660G= | GRCh38 |
NC_000023.10:g.68049503G= , CM000685.1:g.68049503G= | GRCh37 |
NC_000023.9:g.67966228G= | NCBI36 |
NG_008887.1:g.5664G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000204961.5:c.-117G= MANE Select | ENSP00000204961.4:n.-117G= | |
ENST00000204961.4:c.-117G= | ENSP00000204961.4:n.-117G= | |
NM_004429.4:c.-117G= | NP_004420.1:n.-117G= | |
NM_004429.5:c.-117G= MANE Select | NP_004420.1:n.-117G= |