HGVS | Genome Assembly |
---|---|
NC_000005.10:g.174221371T>C , CM000667.2:g.174221371T>C | GRCh38 |
NC_000005.9:g.173648374T>C , CM000667.1:g.173648374T>C | GRCh37 |
NC_000005.8:g.173580980T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000521585.5:c.*18+16067T>C | ENSP00000429863.1:n.*18+16067T>C |