HGVS | Genome Assembly |
---|---|
NC_000004.12:g.38811385T= , CM000666.2:g.38811385T= | GRCh38 |
NC_000004.11:g.38813006T= , CM000666.1:g.38813006T= | GRCh37 |
NC_000004.10:g.38489401T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000506146.5:c.-352-6192A= | ENSP00000423725.1:n.-352-6192A= |