HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17401529T= , CM000663.2:g.17401529T= | GRCh38 |
NC_000001.10:g.17728025T= , CM000663.1:g.17728025T= | GRCh37 |
NC_000001.9:g.17600612T= | NCBI36 |
NG_032943.1:g.34284T= | |
NG_032943.2:g.34284T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000619609.1:c.*91T= MANE Select | ENSP00000483125.1:n.*91T= | |
NM_207421.4:c.*91T= MANE Select | NP_997304.3:n.*91T= |