dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.127081052C>A , CM000670.2:g.127081052C>A | GRCh38 |
| NC_000008.10:g.128093297C>A , CM000670.1:g.128093297C>A | GRCh37 |
| NC_000008.9:g.128162479C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_109833.1:n.1179C>A (PRNCR1) | ||
| NR_119373.1:n.101+1069G>T (PCAT2) |