HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91111794C>T , CM000674.2:g.91111794C>T | GRCh38 |
NC_000012.11:g.91505571C>T , CM000674.1:g.91505571C>T | GRCh37 |
NC_000012.10:g.90029702C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266718.4:c.-418G>A | ENSP00000266718.4:n.-418G>A |