HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94111517A= , CM000663.2:g.94111517A= | GRCh38 |
NC_000001.10:g.94577073A= , CM000663.1:g.94577073A= | GRCh37 |
NC_000001.9:g.94349661A= | NCBI36 |
NG_009073.1:g.14633T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.223T= MANE Select | ENSP00000359245.3:p.Cys75= | |
ENST00000649773.1:c.223T= | ENSP00000496882.1:p.Cys75= | |
ENST00000370225.3:c.223T= | ENSP00000359245.3:p.Cys75= | |
NM_000350.2:c.223T= | NP_000341.2:p.Cys75= | |
NM_000350.3:c.223T= MANE Select | NP_000341.2:p.Cys75= |