Linked Data
gnomAD v4:
8-127401199-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.127401199C>A , CM000670.2:g.127401199C>A | GRCh38 |
| NC_000008.10:g.128413444C>A , CM000670.1:g.128413444C>A | GRCh37 |
| NC_000008.9:g.128482626C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645438.1:c.-559-13689C>A (POU5F1B) | ENSP00000495779.1:n.-559-13689C>A | |
| NR_109834.1:n.801C>A (CCAT2) | ||
| NR_117100.1:n.1176+19630G>T (CASC8) |