HGVS | Genome Assembly |
---|---|
NC_000001.11:g.119667132T>C , CM000663.2:g.119667132T>C | GRCh38 |
NC_000001.10:g.120209755T>C , CM000663.1:g.120209755T>C | GRCh37 |
NC_000001.9:g.120011278T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000641597.1:c.-615-2062T>C | ENSP00000493382.1:n.-615-2062T>C | |
ENST00000493622.5:n.117-2059T>C |