Linked Data
dbSNP Id:
rs1858690527
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.61392355T>C , CM000673.2:g.61392355T>C | GRCh38 |
| NC_000011.9:g.61159827T>C , CM000673.1:g.61159827T>C | GRCh37 |
| NC_000011.8:g.60916403T>C | NCBI36 |
| NG_032976.1:g.4996T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000515837.6:c.-277T>C | ENSP00000440638.1:n.-277T>C | |
| XM_005274039.3:c.-608T>C | XP_005274096.1:n.-608T>C | |
| XM_005274039.4:c.-608T>C | XP_005274096.1:n.-608T>C |