HGVS | Genome Assembly |
---|---|
NC_000005.10:g.63960003A= , CM000667.2:g.63960003A= | GRCh38 |
NC_000005.9:g.63255830A= , CM000667.1:g.63255830A= | GRCh37 |
NC_000005.8:g.63291586A= | NCBI36 |
NG_032816.1:g.7290T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000323865.5:c.*448T= MANE Select | ENSP00000316244.4:n.*448T= | |
NM_000524.4:c.*448T= MANE Select | NP_000515.2:n.*448T= |