HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169532508A>G , CM000663.2:g.169532508A>G | GRCh38 |
NC_000001.10:g.169501746A>G , CM000663.1:g.169501746A>G | GRCh37 |
NC_000001.9:g.167768370A>G | NCBI36 |
NG_011806.1:g.59024T>C , LRG_553:g.59024T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000367797.9:c.4972-1486T>C MANE Select | ENSP00000356771.3:n.4972-1486T>C | |
ENST00000367796.3:c.4987-1486T>C | ENSP00000356770.3:n.4987-1486T>C | |
ENST00000367797.7:c.4972-1486T>C | ENSP00000356771.3:n.4972-1486T>C | |
NM_000130.4:c.4972-1486T>C , LRG_553t1:c.4972-1486T>C | NP_000121.2:n.4972-1486T>C | |
XM_017000660.2:c.4561-1486T>C | XP_016856149.1:n.4561-1486T>C | |
NM_000130.5:c.4972-1486T>C MANE Select | NP_000121.2:n.4972-1486T>C |