HGVS | Genome Assembly |
---|---|
NC_000024.10:g.641000C>T , CM000686.2:g.641000C>T | GRCh38 |
NC_000024.9:g.551735C>T , CM000686.1:g.551735C>T | GRCh37 |
NC_000024.8:g.521735C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000711141.1:c.546C>T | ENSP00000518639.1:p.Gly182= | |
ENST00000711142.1:c.546C>T | ENSP00000518640.1:p.Gly182= | |
ENST00000711143.1:c.546C>T | ENSP00000518641.1:p.Gly182= | |
ENST00000711145.1:c.546C>T | ENSP00000518642.1:p.Gly182= |