HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31172293T>A , CM000668.2:g.31172293T>A | GRCh38 |
NC_000006.11:g.31140070T>A , CM000668.1:g.31140070T>A | GRCh37 |
NC_000006.10:g.31248049T>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000441888.7:c.-183-6246A>T | ENSP00000389359.2:n.-183-6246A>T |