HGVS | Genome Assembly |
---|---|
NC_000015.10:g.65077597A>T , CM000677.2:g.65077597A>T | GRCh38 |
NC_000015.9:g.65369935A>T , CM000677.1:g.65369935A>T | GRCh37 |
NC_000015.8:g.63156988A>T | NCBI36 |
NG_021411.1:g.5782A>T , LRG_682:g.5782A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000432196.5:c.782A>T MANE Select | ENSP00000388723.2:p.Tyr261Phe | |
ENST00000432196.3:c.782A>T | ENSP00000388723.2:p.Tyr261Phe | |
NM_001101362.2:c.782A>T , LRG_682t1:c.782A>T | NP_001094832.1:p.Tyr261Phe | |
NM_001101362.3:c.782A>T MANE Select | NP_001094832.1:p.Tyr261Phe |