HGVS | Genome Assembly |
---|---|
NC_000016.10:g.81357925T>A , CM000678.2:g.81357925T>A | GRCh38 |
NC_000016.9:g.81391530T>A , CM000678.1:g.81391530T>A | GRCh37 |
NC_000016.8:g.79949031T>A | NCBI36 |
NG_009007.1:g.47960T>A , LRG_242:g.47960T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648349.2:c.*675T>A | ENSP00000498114.1:n.*675T>A | |
ENST00000648994.2:c.967T>A MANE Select | ENSP00000497351.1:p.Ser323Thr | |
ENST00000650388.1:c.501T>A | ENSP00000498081.1:n.501T>A | |
ENST00000568107.2:c.967T>A | ENSP00000476795.1:p.Ser323Thr | |
NM_022041.3:c.967T>A , LRG_242t1:c.967T>A | NP_071324.1:p.Ser323Thr | |
XM_017023734.1:c.328T>A | XP_016879223.1:p.Ser110Thr | |
NM_001377486.1:c.328T>A | NP_001364415.1:p.Ser110Thr | |
NM_022041.4:c.967T>A MANE Select | NP_071324.1:p.Ser323Thr |