HGVS | Genome Assembly |
---|---|
NC_000006.12:g.22139917A>C , CM000668.2:g.22139917A>C | GRCh38 |
NC_000006.11:g.22140146A>C , CM000668.1:g.22140146A>C | GRCh37 |
NC_000006.10:g.22248125A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_015410.1:n.1391+28997A>C (CASC15) | ||
NR_034143.1:n.228-3248T>G (NBAT1) | ||
NR_015410.2:n.1422+28997A>C (CASC15) |