HGVS | Genome Assembly |
---|---|
NC_000001.11:g.230702512G= , CM000663.2:g.230702512G= | GRCh38 |
NC_000001.10:g.230838258G= , CM000663.1:g.230838258G= | GRCh37 |
NC_000001.9:g.228904881G= | NCBI36 |
NG_008836.1:g.17079C= | |
NG_008836.2:g.17079C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000679738.1:c.*629C= | ENSP00000505063.1:n.*629C= | |
ENST00000679802.1:c.*1519C= | ENSP00000505184.1:n.*1519C= | |
ENST00000679854.1:n.6365C= | ||
ENST00000680041.1:c.*629C= | ENSP00000504866.1:n.*629C= | |
ENST00000680783.1:c.829+7483C= | ENSP00000506329.1:n.829+7483C= | |
ENST00000681347.1:n.4166C= | ||
ENST00000681514.1:c.*629C= | ENSP00000505963.1:n.*629C= | |
ENST00000681772.1:c.*1554C= | ENSP00000505829.1:n.*1554C= |