Linked Data
dbSNP Id:
rs1848318964
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.91588299T>C , CM000672.2:g.91588299T>C | GRCh38 |
| NC_000010.10:g.93348056T>C , CM000672.1:g.93348056T>C | GRCh37 |
| NC_000010.9:g.93338036T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_024467.1:n.110+23052A>G |