HGVS | Genome Assembly |
---|---|
NC_000016.10:g.2317763T= , CM000678.2:g.2317763T= | GRCh38 |
NC_000016.9:g.2367764T= , CM000678.1:g.2367764T= | GRCh37 |
NC_000016.8:g.2307765T= | NCBI36 |
NG_011790.1:g.27984A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301732.10:c.875A= MANE Select | ENSP00000301732.5:p.Glu292= | |
ENST00000301732.9:c.875A= | ENSP00000301732.5:p.Glu292= | |
ENST00000382381.7:c.875A= | ENSP00000371818.3:p.Glu292= | |
ENST00000563623.5:n.1438A= | ||
NM_001089.2:c.875A= | NP_001080.2:p.Glu292= | |
NM_001089.3:c.875A= MANE Select | NP_001080.2:p.Glu292= |