HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94007632A>T , CM000663.2:g.94007632A>T | GRCh38 |
NC_000001.10:g.94473188A>T , CM000663.1:g.94473188A>T | GRCh37 |
NC_000001.9:g.94245776A>T | NCBI36 |
NG_009073.1:g.118518T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000370225.4:c.6005+2T>A MANE Select | ENSP00000359245.3:n.6005+2T>A | |
ENST00000370225.3:c.6005+2T>A | ENSP00000359245.3:n.6005+2T>A | |
ENST00000465352.1:n.421+2T>A | ||
ENST00000484388.1:n.119+2T>A | ||
ENST00000536513.5:c.2381+2T>A | ENSP00000439707.2:n.2381+2T>A | |
NM_000350.2:c.6005+2T>A | NP_000341.2:n.6005+2T>A | |
NM_000350.3:c.6005+2T>A MANE Select | NP_000341.2:n.6005+2T>A |