HGVS | Genome Assembly |
---|---|
NC_000023.11:g.120626964C= , CM000685.2:g.120626964C= | GRCh38 |
NC_000023.10:g.119760819C= , CM000685.1:g.119760819C= | GRCh37 |
NC_000023.9:g.119644847C= | NCBI36 |
NG_016219.1:g.8187G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000304661.6:c.203G= MANE Select | ENSP00000304364.5:p.Arg68= | |
ENST00000304661.5:c.203G= | ENSP00000304364.5:p.Arg68= | |
ENST00000371313.2:c.203G= | ENSP00000360363.2:p.Arg68= | |
NM_001011551.2:c.203G= | NP_001011551.1:p.Arg68= | |
NM_152692.4:c.203G= | NP_689905.1:p.Arg68= | |
NM_001011551.3:c.203G= MANE Select | NP_001011551.1:p.Arg68= | |
NM_152692.5:c.203G= | NP_689905.1:p.Arg68= |