HGVS | Genome Assembly |
---|---|
NC_000015.10:g.65077686C= , CM000677.2:g.65077686C= | GRCh38 |
NC_000015.9:g.65370024C= , CM000677.1:g.65370024C= | GRCh37 |
NC_000015.8:g.63157077C= | NCBI36 |
NG_021411.1:g.5871C= , LRG_682:g.5871C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000432196.5:c.871C= MANE Select | ENSP00000388723.2:p.Leu291= | |
ENST00000432196.3:c.871C= | ENSP00000388723.2:p.Leu291= | |
NM_001101362.2:c.871C= , LRG_682t1:c.871C= | NP_001094832.1:p.Leu291= | |
NM_001101362.3:c.871C= MANE Select | NP_001094832.1:p.Leu291= |