Linked Data
dbSNP Id:
rs1881403152
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.78451854T>C , CM000675.2:g.78451854T>C | GRCh38 |
| NC_000013.10:g.79025989T>C , CM000675.1:g.79025989T>C | GRCh37 |
| NC_000013.9:g.77923990T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_047001.1:n.385-153447T>C |