HGVS | Genome Assembly |
---|---|
NC_000006.12:g.33075560A= , CM000668.2:g.33075560A= | GRCh38 |
NC_000006.11:g.33043337A= , CM000668.1:g.33043337A= | GRCh37 |
NC_000006.10:g.33151315A= | NCBI36 |
NG_033241.1:g.10219T= | |
NG_033242.1:g.4635A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000417724.1:c.-140-1850T= | ENSP00000398134.1:n.-140-1850T= | |
ENST00000419277.5:c.-99-1891T= | ENSP00000393566.1:n.-99-1891T= | |
ENST00000453337.1:c.-202-1788T= | ENSP00000390929.1:n.-202-1788T= | |
ENST00000476642.5:n.76+5120T= | ||
NM_001242524.1:c.-99-1891T= | NP_001229453.1:n.-99-1891T= | |
NM_001242525.1:c.-23-1967T= | NP_001229454.1:n.-23-1967T= | |
NM_001242524.2:c.-99-1891T= | NP_001229453.1:n.-99-1891T= | |
NM_001242525.2:c.-23-1967T= | NP_001229454.1:n.-23-1967T= |