Linked Data
dbSNP Id:
rs1762077295
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.22139784C>A , CM000668.2:g.22139784C>A | GRCh38 |
| NC_000006.11:g.22140013C>A , CM000668.1:g.22140013C>A | GRCh37 |
| NC_000006.10:g.22247992C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_015410.1:n.1391+28864C>A (CASC15) | ||
| NR_034143.1:n.228-3115G>T (NBAT1) | ||
| NR_015410.2:n.1422+28864C>A (CASC15) |