HGVS | Genome Assembly |
---|---|
NC_000005.10:g.132868703A= , CM000667.2:g.132868703A= | GRCh38 |
NC_000005.9:g.132204395A= , CM000667.1:g.132204395A= | GRCh37 |
NC_000005.8:g.132232294A= | NCBI36 |
NG_012221.1:g.7077A= | |
NG_047051.1:g.3182T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378670.8:c.*1121A= MANE Select | ENSP00000367939.3:n.*1121A= | |
NM_014402.4:c.*1121A= | NP_055217.2:n.*1121A= | |
NM_014402.5:c.*1121A= MANE Select | NP_055217.2:n.*1121A= |