HGVS | Genome Assembly |
---|---|
NC_000011.10:g.110460816G= , CM000673.2:g.110460816G= | GRCh38 |
NC_000011.9:g.110331540G= , CM000673.1:g.110331540G= | GRCh37 |
NC_000011.8:g.109836750G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260270.3:c.441-1538G= MANE Select | ENSP00000260270.2:n.441-1538G= | |
ENST00000260270.2:c.441-1538G= | ENSP00000260270.2:n.441-1538G= | |
NM_004109.4:c.441-1538G= | NP_004100.1:n.441-1538G= | |
NM_004109.5:c.441-1538G= MANE Select | NP_004100.1:n.441-1538G= |