HGVS | Genome Assembly |
---|---|
NC_000002.12:g.169487826T= , CM000664.2:g.169487826T= | GRCh38 |
NC_000002.11:g.170344336T= , CM000664.1:g.170344336T= | GRCh37 |
NC_000002.10:g.170052582T= | NCBI36 |
NG_011567.1:g.13331T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295240.8:c.229T= MANE Select | ENSP00000295240.3:p.Leu77= | |
ENST00000295240.7:c.229T= | ENSP00000295240.3:p.Leu77= | |
ENST00000392663.6:c.229T= | ENSP00000376431.2:p.Leu77= | |
ENST00000443151.1:c.143-161T= | ENSP00000406182.1:n.143-161T= | |
ENST00000475571.1:n.65T= | ||
ENST00000513963.1:c.229T= | ENSP00000424363.1:p.Leu77= | |
NM_152384.2:c.229T= | NP_689597.1:p.Leu77= | |
NM_152384.3:c.229T= MANE Select | NP_689597.1:p.Leu77= |