Linked Data
dbSNP Id:
rs1586652000
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.128529801T>C , CM000670.2:g.128529801T>C | GRCh38 |
| NC_000008.10:g.129542047T>C , CM000670.1:g.129542047T>C | GRCh37 |
| NC_000008.9:g.129611229T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_121672.1:n.508+31269A>G |