HGVS | Genome Assembly |
---|---|
NC_000006.12:g.24146131T= , CM000668.2:g.24146131T= | GRCh38 |
NC_000006.11:g.24146359T= , CM000668.1:g.24146359T= | GRCh37 |
NC_000006.10:g.24254338T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378491.9:c.*185T= MANE Select | ENSP00000367752.4:n.*185T= | |
ENST00000378478.5:c.*185T= | ENSP00000367739.2:n.*185T= | |
ENST00000378491.8:c.*185T= | ENSP00000367752.4:n.*185T= | |
ENST00000468195.2:n.257-8640T= | ||
NM_080723.4:c.*185T= | NP_542454.3:n.*185T= | |
NM_080723.5:c.*185T= MANE Select | NP_542454.3:n.*185T= |