HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86739660A= , CM000670.2:g.86739660A= | GRCh38 |
NC_000008.10:g.87751888A= , CM000670.1:g.87751888A= | GRCh37 |
NC_000008.9:g.87821004A= | NCBI36 |
NG_016980.1:g.9016T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320005.6:c.206T= MANE Select | ENSP00000316605.5:p.Ile69= | |
ENST00000681746.1:c.206T= | ENSP00000505959.1:p.Ile69= | |
ENST00000320005.5:c.206T= | ENSP00000316605.5:p.Ile69= | |
ENST00000519777.1:n.188T= | ||
NM_019098.4:c.206T= | NP_061971.3:p.Ile69= | |
NM_019098.5:c.206T= MANE Select | NP_061971.3:p.Ile69= |