HGVS | Genome Assembly |
---|---|
NC_000004.12:g.38811398C>T , CM000666.2:g.38811398C>T | GRCh38 |
NC_000004.11:g.38813019C>T , CM000666.1:g.38813019C>T | GRCh37 |
NC_000004.10:g.38489414C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000506146.5:c.-352-6205G>A | ENSP00000423725.1:n.-352-6205G>A |