Linked Data
gnomAD v4:
8-127080222-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.127080222C>A , CM000670.2:g.127080222C>A | GRCh38 |
| NC_000008.10:g.128092467C>A , CM000670.1:g.128092467C>A | GRCh37 |
| NC_000008.9:g.128161649C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_109833.1:n.349C>A (PRNCR1) | ||
| NR_119373.1:n.102-1089G>T (PCAT2) |