HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31171675T>C , CM000668.2:g.31171675T>C | GRCh38 |
NC_000006.11:g.31139452T>C , CM000668.1:g.31139452T>C | GRCh37 |
NC_000006.10:g.31247431T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000441888.7:c.-183-5628A>G | ENSP00000389359.2:n.-183-5628A>G |