HGVS | Genome Assembly |
---|---|
NC_000013.11:g.39776775T= , CM000675.2:g.39776775T= | GRCh38 |
NC_000013.10:g.40350912T= , CM000675.1:g.40350912T= | GRCh37 |
NC_000013.9:g.39248912T= | NCBI36 |
NG_028352.1:g.126149T= |
HGVS | Amino-acid Change |
---|---|
NM_001145079.1:c.1827-11560T= | NP_001138551.1:n.1827-11560T= |
NM_001145079.2:c.1827-11560T= | NP_001138551.1:n.1827-11560T= |
ENST00000416691.5:c.1827-11560T= | ENSP00000403733.1:n.1827-11560T= |