HGVS | Genome Assembly |
---|---|
NC_000010.11:g.46046570T= , CM000672.2:g.46046570T= | GRCh38 |
NC_000010.10:g.51549252A= , CM000672.1:g.51549252A= | GRCh37 |
NC_000010.9:g.51219258A= | NCBI36 |
NG_011551.1:g.4700A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000663171.1:c.-142-191A= | ENSP00000499419.1:n.-142-191A= |