HGVS | Genome Assembly |
---|---|
NC_000001.11:g.93997868A= , CM000663.2:g.93997868A= | GRCh38 |
NC_000001.10:g.94463424A= , CM000663.1:g.94463424A= | GRCh37 |
NC_000001.9:g.94236012A= | NCBI36 |
NG_009073.1:g.128282T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.6722T= MANE Select | ENSP00000359245.3:p.Leu2241= | |
ENST00000370225.3:c.6722T= | ENSP00000359245.3:p.Leu2241= | |
ENST00000536513.5:c.3098T= | ENSP00000439707.2:p.Leu1033= | |
NM_000350.2:c.6722T= | NP_000341.2:p.Leu2241= | |
NM_000350.3:c.6722T= MANE Select | NP_000341.2:p.Leu2241= |