HGVS | Genome Assembly |
---|---|
NC_000006.12:g.33092566C>T , CM000668.2:g.33092566C>T | GRCh38 |
NC_000006.11:g.33060343C>T , CM000668.1:g.33060343C>T | GRCh37 |
NC_000006.10:g.33168321C>T | NCBI36 |
NG_033242.1:g.21641C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000433582.1:n.301-166G>A |