HGVS | Genome Assembly |
---|---|
NC_000015.10:g.65077622G>T , CM000677.2:g.65077622G>T | GRCh38 |
NC_000015.9:g.65369960G>T , CM000677.1:g.65369960G>T | GRCh37 |
NC_000015.8:g.63157013G>T | NCBI36 |
NG_021411.1:g.5807G>T , LRG_682:g.5807G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000432196.5:c.807G>T MANE Select | ENSP00000388723.2:p.Arg269Ser | |
ENST00000432196.3:c.807G>T | ENSP00000388723.2:p.Arg269Ser | |
NM_001101362.2:c.807G>T , LRG_682t1:c.807G>T | NP_001094832.1:p.Arg269Ser | |
NM_001101362.3:c.807G>T MANE Select | NP_001094832.1:p.Arg269Ser |