Linked Data
dbSNP Id:
rs1869949448
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.111398904T>C , CM000674.2:g.111398904T>C | GRCh38 |
| NC_000012.11:g.111836708T>C , CM000674.1:g.111836708T>C | GRCh37 |
| NC_000012.10:g.110321091T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_945342.1:n.44+2031T>C |