HGVS | Genome Assembly |
---|---|
NC_000015.10:g.90501200C= , CM000677.2:g.90501200C= | GRCh38 |
NC_000015.9:g.91044432C= , CM000677.1:g.91044432C= | GRCh37 |
NC_000015.8:g.88845436C= | NCBI36 |
NG_052946.1:g.117960C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000268182.10:c.*1092C= MANE Select | ENSP00000268182.5:n.*1092C= | |
ENST00000268182.9:c.*1092C= | ENSP00000268182.5:n.*1092C= | |
ENST00000558957.1:n.2124C= | ||
ENST00000561086.1:n.1833C= | ||
NM_003870.3:c.*1092C= | NP_003861.1:n.*1092C= | |
XR_001751409.2:n.6195C= | ||
NM_003870.4:c.*1092C= MANE Select | NP_003861.1:n.*1092C= |