HGVS | Genome Assembly |
---|---|
NC_000014.9:g.74493533T= , CM000676.2:g.74493533T= | GRCh38 |
NC_000014.8:g.74960236T= , CM000676.1:g.74960236T= | GRCh37 |
NC_000014.7:g.74029989T= | NCBI36 |
NG_007117.1:g.4849A= | |
NG_033074.1:g.4814T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000555592.1:c.-64+37A= | ENSP00000450887.1:n.-64+37A= | |
ENST00000556009.5:c.147+498A= |