Linked Data
dbSNP Id:
rs970333565
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.117524904G>C , CM000672.2:g.117524904G>C | GRCh38 |
| NC_000010.10:g.119284415G>C , CM000672.1:g.119284415G>C | GRCh37 |
| NC_000010.9:g.119274405G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_002791.2:n.574+19402C>G | ||
| NR_144378.1:n.493+17193C>G |