Linked Data
gnomAD v4:
8-127080219-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.127080219T>C , CM000670.2:g.127080219T>C | GRCh38 |
| NC_000008.10:g.128092464T>C , CM000670.1:g.128092464T>C | GRCh37 |
| NC_000008.9:g.128161646T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_109833.1:n.346T>C (PRNCR1) | ||
| NR_119373.1:n.102-1086A>G (PCAT2) |