HGVS | Genome Assembly |
---|---|
NC_000020.11:g.46011739C= , CM000682.2:g.46011739C= | GRCh38 |
NC_000020.10:g.44640378C= , CM000682.1:g.44640378C= | GRCh37 |
NC_000020.9:g.44073785C= | NCBI36 |
NG_011468.1:g.7832C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372330.3:c.989C= MANE Select | ENSP00000361405.3:p.Pro330= | |
NM_004994.2:c.989C= | NP_004985.2:p.Pro330= | |
NM_004994.3:c.989C= MANE Select | NP_004985.2:p.Pro330= |