HGVS | Genome Assembly |
---|---|
NC_000004.12:g.38811394G>T , CM000666.2:g.38811394G>T | GRCh38 |
NC_000004.11:g.38813015G>T , CM000666.1:g.38813015G>T | GRCh37 |
NC_000004.10:g.38489410G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000506146.5:c.-352-6201C>A | ENSP00000423725.1:n.-352-6201C>A |