HGVS | Genome Assembly |
---|---|
NC_000018.10:g.60371292T= , CM000680.2:g.60371292T= | GRCh38 |
NC_000018.9:g.58038525T= , CM000680.1:g.58038525T= | GRCh37 |
NC_000018.8:g.56189505T= | NCBI36 |
NG_016441.1:g.6477A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299766.5:c.*59A= MANE Select | ENSP00000299766.3:n.*59A= | |
ENST00000299766.4:c.*59A= | ENSP00000299766.3:n.*59A= | |
NM_005912.3:c.*59A= MANE Select | NP_005903.2:n.*59A= |