HGVS | Genome Assembly |
---|---|
NC_000005.10:g.67184088A= , CM000667.2:g.67184088A= | GRCh38 |
NC_000005.9:g.66479916A= , CM000667.1:g.66479916A= | GRCh37 |
NC_000005.8:g.66515672A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256447.5:c.755T= MANE Select | ENSP00000256447.4:p.Leu252= | |
NM_005582.2:c.755T= | NP_005573.2:p.Leu252= | |
XM_005248504.3:c.716T= | XP_005248561.1:p.Leu239= | |
XM_005248504.4:c.716T= | XP_005248561.1:p.Leu239= | |
NM_005582.3:c.755T= MANE Select | NP_005573.2:p.Leu252= |