HGVS | Genome Assembly |
---|---|
NC_000014.9:g.74493540T= , CM000676.2:g.74493540T= | GRCh38 |
NC_000014.8:g.74960243T= , CM000676.1:g.74960243T= | GRCh37 |
NC_000014.7:g.74029996T= | NCBI36 |
NG_007117.1:g.4842A= | |
NG_033074.1:g.4821T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000555592.1:c.-64+30A= | ENSP00000450887.1:n.-64+30A= | |
ENST00000556009.5:c.147+491A= |