Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.127080326T>C , CM000670.2:g.127080326T>C | GRCh38 |
| NC_000008.10:g.128092571T>C , CM000670.1:g.128092571T>C | GRCh37 |
| NC_000008.9:g.128161753T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_109833.1:n.453T>C (PRNCR1) | ||
| NR_119373.1:n.102-1193A>G (PCAT2) |