Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.22139638T>C , CM000668.2:g.22139638T>C | GRCh38 |
| NC_000006.11:g.22139867T>C , CM000668.1:g.22139867T>C | GRCh37 |
| NC_000006.10:g.22247846T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_015410.1:n.1391+28718T>C (CASC15) | ||
| NR_034143.1:n.228-2969A>G (NBAT1) | ||
| NR_015410.2:n.1422+28718T>C (CASC15) |