HGVS | Genome Assembly |
---|---|
NC_000006.12:g.24146029T= , CM000668.2:g.24146029T= | GRCh38 |
NC_000006.11:g.24146257T= , CM000668.1:g.24146257T= | GRCh37 |
NC_000006.10:g.24254236T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378491.9:c.*83T= MANE Select | ENSP00000367752.4:n.*83T= | |
ENST00000378478.5:c.*83T= | ENSP00000367739.2:n.*83T= | |
ENST00000378491.8:c.*83T= | ENSP00000367752.4:n.*83T= | |
ENST00000468195.2:n.257-8742T= | ||
NM_080723.4:c.*83T= | NP_542454.3:n.*83T= | |
NM_080723.5:c.*83T= MANE Select | NP_542454.3:n.*83T= |