HGVS | Genome Assembly |
---|---|
NC_000016.10:g.67437038A= , CM000678.2:g.67437038A= | GRCh38 |
NC_000016.9:g.67470941A= , CM000678.1:g.67470941A= | GRCh37 |
NC_000016.8:g.66028442A= | NCBI36 |
NG_011482.1:g.49149T= | |
NG_016549.1:g.10906A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000326152.6:c.*35A= MANE Select | ENSP00000316786.5:n.*35A= | |
ENST00000326152.5:c.*35A= | ENSP00000316786.5:n.*35A= | |
NM_000196.3:c.*35A= | NP_000187.3:n.*35A= | |
NM_000196.4:c.*35A= MANE Select | NP_000187.3:n.*35A= |