HGVS | Genome Assembly |
---|---|
NC_000022.11:g.20887992G= , CM000684.2:g.20887992G= | GRCh38 |
NC_000022.10:g.21242280G= , CM000684.1:g.21242280G= | GRCh37 |
NC_000022.9:g.19572280G= | NCBI36 |
NG_012152.1:g.33989G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000215730.12:c.*156G= MANE Select | ENSP00000215730.6:n.*156G= | |
ENST00000215730.11:c.*156G= | ENSP00000215730.6:n.*156G= | |
NM_004782.3:c.*156G= | NP_004773.1:n.*156G= | |
NM_004782.4:c.*156G= MANE Select | NP_004773.1:n.*156G= |