Linked Data
gnomAD v4:
8-127080144-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.127080144C>T , CM000670.2:g.127080144C>T | GRCh38 |
| NC_000008.10:g.128092389C>T , CM000670.1:g.128092389C>T | GRCh37 |
| NC_000008.9:g.128161571C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_109833.1:n.271C>T (PRNCR1) | ||
| NR_119373.1:n.102-1011G>A (PCAT2) |