HGVS | Genome Assembly |
---|---|
NC_000024.10:g.641050A= , CM000686.2:g.641050A= | GRCh38 |
NC_000024.9:g.551785A= , CM000686.1:g.551785A= | GRCh37 |
NC_000024.8:g.521785A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000711141.1:c.596A= | ENSP00000518639.1:p.Tyr199= | |
ENST00000711142.1:c.596A= | ENSP00000518640.1:p.Tyr199= | |
ENST00000711143.1:c.596A= | ENSP00000518641.1:p.Tyr199= | |
ENST00000711145.1:c.596A= | ENSP00000518642.1:p.Tyr199= |