HGVS | Genome Assembly |
---|---|
NC_000001.11:g.186680450T>C , CM000663.2:g.186680450T>C | GRCh38 |
NC_000001.10:g.186649582T>C , CM000663.1:g.186649582T>C | GRCh37 |
NC_000001.9:g.184916205T>C | NCBI36 |
NG_028206.2:g.4978A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000680451.1:c.-113-47A>G | ENSP00000506242.1:n.-113-47A>G |