HGVS | Genome Assembly |
---|---|
NC_000020.11:g.10658387A= , CM000682.2:g.10658387A= | GRCh38 |
NC_000020.10:g.10639035A= , CM000682.1:g.10639035A= | GRCh37 |
NC_000020.9:g.10587035A= | NCBI36 |
NG_007496.1:g.20660T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254958.10:c.694+81T= MANE Select | ENSP00000254958.4:n.694+81T= | |
ENST00000254958.9:c.694+81T= | ENSP00000254958.4:n.694+81T= | |
ENST00000423891.6:n.560+81T= | ||
NM_000214.2:c.694+81T= | NP_000205.1:n.694+81T= | |
NM_000214.3:c.694+81T= MANE Select | NP_000205.1:n.694+81T= |