HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31172258C>T , CM000668.2:g.31172258C>T | GRCh38 |
NC_000006.11:g.31140035C>T , CM000668.1:g.31140035C>T | GRCh37 |
NC_000006.10:g.31248014C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000441888.7:c.-183-6211G>A | ENSP00000389359.2:n.-183-6211G>A |