Linked Data
dbSNP Id:
rs1941618395
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116840040C>T , CM000673.2:g.116840040C>T | GRCh38 |
| NC_000011.9:g.116710756C>T , CM000673.1:g.116710756C>T | GRCh37 |
| NC_000011.8:g.116215966C>T | NCBI36 |
| NG_012021.1:g.2583G>A , LRG_767:g.2583G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_126362.1:n.123+3801C>T |