HGVS | Genome Assembly |
---|---|
NC_000006.12:g.22139806C>T , CM000668.2:g.22139806C>T | GRCh38 |
NC_000006.11:g.22140035C>T , CM000668.1:g.22140035C>T | GRCh37 |
NC_000006.10:g.22248014C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_015410.1:n.1391+28886C>T (CASC15) | ||
NR_034143.1:n.228-3137G>A (NBAT1) | ||
NR_015410.2:n.1422+28886C>T (CASC15) |