HGVS | Genome Assembly |
---|---|
NC_000011.10:g.763805T= , CM000673.2:g.763805T= | GRCh38 |
NC_000011.9:g.763805T= , CM000673.1:g.763805T= | GRCh37 |
NC_000011.8:g.753805T= | NCBI36 |
NG_008160.1:g.21374T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000319006.8:c.696T= MANE Select | ENSP00000321259.3:p.Ile232= | |
ENST00000319006.7:c.696T= | ENSP00000321259.3:p.Ile232= | |
ENST00000528097.5:c.696T= | ENSP00000437098.1:p.Ile232= | |
ENST00000530440.1:c.*355T= | ENSP00000433501.1:n.*355T= | |
NM_006755.1:c.696T= | NP_006746.1:p.Ile232= | |
NM_006755.2:c.696T= MANE Select | NP_006746.1:p.Ile232= |