HGVS | Genome Assembly |
---|---|
NC_000020.11:g.63264568A>C , CM000682.2:g.63264568A>C | GRCh38 |
NC_000020.10:g.61895920A>C , CM000682.1:g.61895920A>C | GRCh37 |
NC_000020.9:g.61366365A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370307.6:c.-133+8014T>G | ENSP00000359330.2:n.-133+8014T>G |