HGVS | Genome Assembly |
---|---|
NC_000017.11:g.56594940C= , CM000679.2:g.56594940C= | GRCh38 |
NC_000017.10:g.54672301C= , CM000679.1:g.54672301C= | GRCh37 |
NC_000017.9:g.52027300C= | NCBI36 |
NG_011958.1:g.6242C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000332822.6:c.*18C= MANE Select | ENSP00000328181.4:n.*18C= | |
ENST00000332822.4:c.*18C= | ENSP00000328181.4:n.*18C= | |
NM_005450.4:c.*18C= | NP_005441.1:n.*18C= | |
NM_005450.6:c.*18C= MANE Select | NP_005441.1:n.*18C= |