Linked Data
dbSNP Id:
rs1248950444
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.127401129C>G , CM000670.2:g.127401129C>G | GRCh38 |
| NC_000008.10:g.128413374C>G , CM000670.1:g.128413374C>G | GRCh37 |
| NC_000008.9:g.128482556C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000645438.1:c.-559-13759C>G (POU5F1B) | ENSP00000495779.1:n.-559-13759C>G | |
| NR_109834.1:n.731C>G (CCAT2) | ||
| NR_117100.1:n.1176+19700G>C (CASC8) |