HGVS | Genome Assembly |
---|---|
NC_000004.12:g.38811127C>A , CM000666.2:g.38811127C>A | GRCh38 |
NC_000004.11:g.38812748C>A , CM000666.1:g.38812748C>A | GRCh37 |
NC_000004.10:g.38489143C>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000506146.5:c.-352-5934G>T | ENSP00000423725.1:n.-352-5934G>T |