HGVS | Genome Assembly |
---|---|
NC_000020.11:g.46011446T>A , CM000682.2:g.46011446T>A | GRCh38 |
NC_000020.10:g.44640085T>A , CM000682.1:g.44640085T>A | GRCh37 |
NC_000020.9:g.44073492T>A | NCBI36 |
NG_011468.1:g.7539T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372330.3:c.824-128T>A MANE Select | ENSP00000361405.3:n.824-128T>A | |
NM_004994.2:c.824-128T>A | NP_004985.2:n.824-128T>A | |
NM_004994.3:c.824-128T>A MANE Select | NP_004985.2:n.824-128T>A |