HGVS | Genome Assembly |
---|---|
NC_000012.12:g.72011400T= , CM000674.2:g.72011400T= | GRCh38 |
NC_000012.11:g.72405180T= , CM000674.1:g.72405180T= | GRCh37 |
NC_000012.10:g.70691447T= | NCBI36 |
NG_008279.1:g.77555T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000333850.4:c.1069-10999T= MANE Select | ENSP00000329093.3:n.1069-10999T= | |
ENST00000333850.3:c.1069-10999T= | ENSP00000329093.3:n.1069-10999T= | |
NM_173353.3:c.1069-10999T= | NP_775489.2:n.1069-10999T= | |
XM_011537899.1:c.475-10999T= | XP_011536201.1:n.475-10999T= | |
NM_173353.4:c.1069-10999T= MANE Select | NP_775489.2:n.1069-10999T= |