Linked Data
gnomAD v4:
8-127079945-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.127079945C>T , CM000670.2:g.127079945C>T | GRCh38 |
| NC_000008.10:g.128092190C>T , CM000670.1:g.128092190C>T | GRCh37 |
| NC_000008.9:g.128161372C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_109833.1:n.72C>T (PRNCR1) | ||
| NR_119373.1:n.102-812G>A (PCAT2) |