HGVS | Genome Assembly |
---|---|
NC_000001.11:g.230702457C= , CM000663.2:g.230702457C= | GRCh38 |
NC_000001.10:g.230838203C= , CM000663.1:g.230838203C= | GRCh37 |
NC_000001.9:g.228904826C= | NCBI36 |
NG_008836.1:g.17134G= | |
NG_008836.2:g.17134G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000679738.1:c.*684G= | ENSP00000505063.1:n.*684G= | |
ENST00000679802.1:c.*1574G= | ENSP00000505184.1:n.*1574G= | |
ENST00000679854.1:n.6420G= | ||
ENST00000680041.1:c.*684G= | ENSP00000504866.1:n.*684G= | |
ENST00000680783.1:c.829+7538G= | ENSP00000506329.1:n.829+7538G= | |
ENST00000681347.1:n.4221G= | ||
ENST00000681514.1:c.*684G= | ENSP00000505963.1:n.*684G= | |
ENST00000681772.1:c.*1609G= | ENSP00000505829.1:n.*1609G= |