Linked Data
dbSNP Id:
rs1941620342
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116840254A>G , CM000673.2:g.116840254A>G | GRCh38 |
| NC_000011.9:g.116710970A>G , CM000673.1:g.116710970A>G | GRCh37 |
| NC_000011.8:g.116216180A>G | NCBI36 |
| NG_012021.1:g.2369T>C , LRG_767:g.2369T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_126362.1:n.123+4015A>G |