HGVS | Genome Assembly |
---|---|
NC_000010.11:g.97611234T= , CM000672.2:g.97611234T= | GRCh38 |
NC_000010.10:g.99370991T= , CM000672.1:g.99370991T= | GRCh37 |
NC_000010.9:g.99360981T= | NCBI36 |
NG_027922.1:g.31890T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370646.9:c.835-276T= MANE Select | ENSP00000359680.4:n.835-276T= | |
ENST00000370646.8:c.835-276T= | ENSP00000359680.4:n.835-276T= | |
ENST00000370647.8:c.346-276T= | ENSP00000359681.4:n.346-276T= | |
ENST00000370649.3:c.345+9244T= | ENSP00000359683.3:n.345+9244T= | |
NM_001134670.1:c.346-276T= | NP_001128142.1:n.346-276T= | |
NM_138413.3:c.835-276T= | NP_612422.2:n.835-276T= | |
NM_138413.4:c.835-276T= MANE Select | NP_612422.2:n.835-276T= | |
NM_001134670.2:c.346-276T= | NP_001128142.1:n.346-276T= |