HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86012784T>C , CM000670.2:g.86012784T>C | GRCh38 |
NC_000008.10:g.87025013T>C , CM000670.1:g.87025013T>C | GRCh37 |
NC_000008.9:g.87094129T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000521564.1:c.-263+25384T>C | ENSP00000429731.1:n.-263+25384T>C |