HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17401537C= , CM000663.2:g.17401537C= | GRCh38 |
NC_000001.10:g.17728033C= , CM000663.1:g.17728033C= | GRCh37 |
NC_000001.9:g.17600620C= | NCBI36 |
NG_032943.1:g.34292C= | |
NG_032943.2:g.34292C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000619609.1:c.*99C= MANE Select | ENSP00000483125.1:n.*99C= | |
NM_207421.4:c.*99C= MANE Select | NP_997304.3:n.*99C= |