Linked Data
dbSNP Id:
rs1411696722
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.127401008G>A , CM000670.2:g.127401008G>A | GRCh38 |
| NC_000008.10:g.128413253G>A , CM000670.1:g.128413253G>A | GRCh37 |
| NC_000008.9:g.128482435G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000645438.1:c.-559-13880G>A (POU5F1B) | ENSP00000495779.1:n.-559-13880G>A | |
| NR_109834.1:n.610G>A (CCAT2) | ||
| NR_117100.1:n.1176+19821C>T (CASC8) |