HGVS | Genome Assembly |
---|---|
NC_000015.10:g.89648738C>T , CM000677.2:g.89648738C>T | GRCh38 |
NC_000015.9:g.90191969C>T , CM000677.1:g.90191969C>T | GRCh37 |
NC_000015.8:g.87992973C>T | NCBI36 |
NG_030338.1:g.11714G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696512.1:c.1083G>A | ENSP00000512678.1:p.Thr361= | |
ENST00000394412.8:c.960G>A MANE Select | ENSP00000377934.3:p.Thr320= | |
ENST00000394412.7:c.960G>A | ENSP00000377934.3:p.Thr320= | |
ENST00000445906.1:c.*619G>A | ENSP00000395906.1:n.*619G>A | |
NM_198525.2:c.960G>A | NP_940927.2:p.Thr320= | |
XM_005254902.2:c.960G>A | XP_005254959.1:p.Thr320= | |
XM_011521531.1:c.1083G>A | XP_011519833.1:p.Thr361= | |
XM_011521532.1:c.1083G>A | XP_011519834.1:p.Thr361= | |
XM_011521533.1:c.1083G>A | XP_011519835.1:p.Thr361= | |
XM_011521534.1:c.1083G>A | XP_011519836.1:p.Thr361= | |
XM_011521535.1:c.1083G>A | XP_011519837.1:p.Thr361= | |
XM_011521536.1:c.1083G>A | XP_011519838.1:p.Thr361= | |
XM_011521537.1:c.1083G>A | XP_011519839.1:p.Thr361= | |
XM_011521531.2:c.1083G>A | XP_011519833.1:p.Thr361= | |
NM_198525.3:c.960G>A MANE Select | NP_940927.2:p.Thr320= |