HGVS | Genome Assembly |
---|---|
NC_000012.12:g.72020700T= , CM000674.2:g.72020700T= | GRCh38 |
NC_000012.11:g.72414480T= , CM000674.1:g.72414480T= | GRCh37 |
NC_000012.10:g.70700747T= | NCBI36 |
NG_008279.1:g.86855T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000333850.4:c.1069-1699T= MANE Select | ENSP00000329093.3:n.1069-1699T= | |
ENST00000333850.3:c.1069-1699T= | ENSP00000329093.3:n.1069-1699T= | |
NM_173353.3:c.1069-1699T= | NP_775489.2:n.1069-1699T= | |
XM_011537899.1:c.475-1699T= | XP_011536201.1:n.475-1699T= | |
NM_173353.4:c.1069-1699T= MANE Select | NP_775489.2:n.1069-1699T= |