HGVS | Genome Assembly |
---|---|
NC_000016.10:g.67436590T= , CM000678.2:g.67436590T= | GRCh38 |
NC_000016.9:g.67470493T= , CM000678.1:g.67470493T= | GRCh37 |
NC_000016.8:g.66027994T= | NCBI36 |
NG_011482.1:g.49597A= | |
NG_016549.1:g.10458T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000326152.6:c.805T= MANE Select | ENSP00000316786.5:p.Ser269= | |
ENST00000326152.5:c.805T= | ENSP00000316786.5:p.Ser269= | |
NM_000196.3:c.805T= | NP_000187.3:p.Ser269= | |
NM_000196.4:c.805T= MANE Select | NP_000187.3:p.Ser269= |