HGVS | Genome Assembly |
---|---|
NC_000012.12:g.5046041T= , CM000674.2:g.5046041T= | GRCh38 |
NC_000012.11:g.5155207T= , CM000674.1:g.5155207T= | GRCh37 |
NC_000012.10:g.5025468T= | NCBI36 |
NG_012198.1:g.7123T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252321.5:c.*52T= MANE Select | ENSP00000252321.3:n.*52T= | |
ENST00000252321.4:c.*52T= | ENSP00000252321.3:n.*52T= | |
NM_002234.3:c.*52T= | NP_002225.2:n.*52T= | |
NM_002234.4:c.*52T= MANE Select | NP_002225.2:n.*52T= |