Linked Data
dbSNP Id:
rs1954584719
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.93586300T>C , CM000674.2:g.93586300T>C | GRCh38 |
| NC_000012.11:g.93980076T>C , CM000674.1:g.93980076T>C | GRCh37 |
| NC_000012.10:g.92504207T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011538935.1:c.591+11127T>C | XP_011537237.1:n.591+11127T>C |