HGVS | Genome Assembly |
---|---|
NC_000001.11:g.207454172T= , CM000663.2:g.207454172T= | GRCh38 |
NC_000001.10:g.207627517T= , CM000663.1:g.207627517T= | GRCh37 |
NC_000001.9:g.205694140T= | NCBI36 |
NG_013006.1:g.4873T= , LRG_348:g.4873T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000699640.1:c.-385+1077T= | ENSP00000514493.1:n.-385+1077T= |