HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154379424G>A , CM000685.2:g.154379424G>A | GRCh38 |
NC_000023.10:g.153607784G>A , CM000685.1:g.153607784G>A | GRCh37 |
NC_000023.9:g.153260978G>A | NCBI36 |
NG_008677.1:g.9989G>A , LRG_745:g.9989G>A | |
NG_011506.1:g.223C>T | |
NG_011506.2:g.215C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682114.1:c.-61G>A | ENSP00000507245.1:n.-61G>A | |
ENST00000369842.9:c.-61G>A MANE Select | ENSP00000358857.4:n.-61G>A | |
ENST00000369835.3:c.-61G>A | ENSP00000358850.3:n.-61G>A | |
ENST00000369842.8:c.-61G>A | ENSP00000358857.4:n.-61G>A | |
ENST00000428228.5:c.-61G>A | ENSP00000401081.1:n.-61G>A | |
ENST00000485261.1:n.21G>A | ||
ENST00000486738.5:n.84G>A | ||
NM_000117.2:c.-61G>A , LRG_745t1:c.-61G>A | NP_000108.1:n.-61G>A | |
XM_024452349.1:c.-269G>A | XP_024308117.1:n.-269G>A | |
NM_000117.3:c.-61G>A MANE Select | NP_000108.1:n.-61G>A |