HGVS | Genome Assembly |
---|---|
NC_000008.11:g.66178664A= , CM000670.2:g.66178664A= | GRCh38 |
NC_000008.10:g.67090899A= , CM000670.1:g.67090899A= | GRCh37 |
NC_000008.9:g.67253453A= | NCBI36 |
NG_016127.1:g.4800T= |
HGVS | Amino-acid Change |
---|---|
ENST00000276571.4:c.-386T= | ENSP00000276571.3:n.-386T= |