Linked Data
dbSNP Id:
rs1649066816
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169736901T>C , CM000663.2:g.169736901T>C | GRCh38 |
| NC_000001.10:g.169706042T>C , CM000663.1:g.169706042T>C | GRCh37 |
| NC_000001.9:g.167972666T>C | NCBI36 |
| NG_012124.1:g.2179A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000498289.5:n.852-46910T>C (FIRRM) | ||
| ENST00000609271.1:c.-201-2778A>G (SELE) | ENSP00000476784.1:n.-201-2778A>G |