HGVS | Genome Assembly |
---|---|
NC_000011.10:g.61798436T>C , CM000673.2:g.61798436T>C | GRCh38 |
NC_000011.9:g.61565908T>C , CM000673.1:g.61565908T>C | GRCh37 |
NC_000011.8:g.61322484T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000574708.5:c.-55+5408T>C | ENSP00000458917.1:n.-55+5408T>C |