HGVS | Genome Assembly |
---|---|
NC_000006.12:g.33092613T>C , CM000668.2:g.33092613T>C | GRCh38 |
NC_000006.11:g.33060390T>C , CM000668.1:g.33060390T>C | GRCh37 |
NC_000006.10:g.33168368T>C | NCBI36 |
NG_033242.1:g.21688T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000433582.1:n.301-213A>G |