HGVS | Genome Assembly |
---|---|
NC_000007.14:g.37952217A>G , CM000669.2:g.37952217A>G | GRCh38 |
NC_000007.13:g.37991819A>G , CM000669.1:g.37991819A>G | GRCh37 |
NC_000007.12:g.37958344A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000447200.2:c.-52-25443T>C | ENSP00000402262.2:n.-52-25443T>C |