HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186085702T= , CM000666.2:g.186085702T= | GRCh38 |
NC_000004.11:g.187006856T= , CM000666.1:g.187006856T= | GRCh37 |
NC_000004.10:g.187243850T= | NCBI36 |
NG_007278.1:g.21548T= , LRG_117:g.21548T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000698352.1:c.*3096T= | ENSP00000513675.1:n.*3096T= | |
ENST00000698353.1:n.3419T= | ||
ENST00000698354.1:c.*829T= | ENSP00000513676.1:n.*829T= | |
ENST00000296795.8:c.*829T= MANE Select | ENSP00000296795.3:n.*829T= | |
ENST00000296795.7:c.*829T= | ENSP00000296795.2:n.*829T= | |
NM_003265.3:c.*829T= MANE Select | NP_003256.1:n.*829T= |