HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154379425C= , CM000685.2:g.154379425C= | GRCh38 |
NC_000023.10:g.153607785C= , CM000685.1:g.153607785C= | GRCh37 |
NC_000023.9:g.153260979C= | NCBI36 |
NG_008677.1:g.9990C= , LRG_745:g.9990C= | |
NG_011506.1:g.222G= | |
NG_011506.2:g.214G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682114.1:c.-60C= | ENSP00000507245.1:n.-60C= | |
ENST00000369842.9:c.-60C= MANE Select | ENSP00000358857.4:n.-60C= | |
ENST00000369835.3:c.-60C= | ENSP00000358850.3:n.-60C= | |
ENST00000369842.8:c.-60C= | ENSP00000358857.4:n.-60C= | |
ENST00000428228.5:c.-60C= | ENSP00000401081.1:n.-60C= | |
ENST00000485261.1:n.22C= | ||
ENST00000486738.5:n.85C= | ||
NM_000117.2:c.-60C= , LRG_745t1:c.-60C= | NP_000108.1:n.-60C= | |
XM_024452349.1:c.-268C= | XP_024308117.1:n.-268C= | |
NM_000117.3:c.-60C= MANE Select | NP_000108.1:n.-60C= |