HGVS | Genome Assembly |
---|---|
NC_000015.10:g.65077417T>A , CM000677.2:g.65077417T>A | GRCh38 |
NC_000015.9:g.65369755T>A , CM000677.1:g.65369755T>A | GRCh37 |
NC_000015.8:g.63156808T>A | NCBI36 |
NG_021411.1:g.5602T>A , LRG_682:g.5602T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000432196.5:c.602T>A MANE Select | ENSP00000388723.2:p.Leu201Gln | |
ENST00000432196.3:c.602T>A | ENSP00000388723.2:p.Leu201Gln | |
NM_001101362.2:c.602T>A , LRG_682t1:c.602T>A | NP_001094832.1:p.Leu201Gln | |
NM_001101362.3:c.602T>A MANE Select | NP_001094832.1:p.Leu201Gln |