Linked Data
dbSNP Id:
rs2139920821
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.22468656C>T , CM000676.2:g.22468656C>T | GRCh38 |
| NC_000014.8:g.22937648C>T , CM000676.1:g.22937648C>T | GRCh37 |
| NC_000014.7:g.22007488C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943593.1:n.776-3370G>A | ||
| XR_943594.1:n.541-3370G>A | ||
| XR_943595.1:n.541-3370G>A | ||
| XR_943596.1:n.776-3370G>A | ||
| NR_148361.1:n.225+12585G>A | ||
| XR_001750629.1:n.292-3370G>A |