HGVS | Genome Assembly |
---|---|
NC_000012.12:g.72020738T>A , CM000674.2:g.72020738T>A | GRCh38 |
NC_000012.11:g.72414518T>A , CM000674.1:g.72414518T>A | GRCh37 |
NC_000012.10:g.70700785T>A | NCBI36 |
NG_008279.1:g.86893T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000333850.4:c.1069-1661T>A MANE Select | ENSP00000329093.3:n.1069-1661T>A | |
ENST00000333850.3:c.1069-1661T>A | ENSP00000329093.3:n.1069-1661T>A | |
NM_173353.3:c.1069-1661T>A | NP_775489.2:n.1069-1661T>A | |
XM_011537899.1:c.475-1661T>A | XP_011536201.1:n.475-1661T>A | |
NM_173353.4:c.1069-1661T>A MANE Select | NP_775489.2:n.1069-1661T>A |