Linked Data
dbSNP Id:
rs10800469
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169736942A>C , CM000663.2:g.169736942A>C | GRCh38 |
| NC_000001.10:g.169706083A>C , CM000663.1:g.169706083A>C | GRCh37 |
| NC_000001.9:g.167972707A>C | NCBI36 |
| NG_012124.1:g.2138T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000498289.5:n.852-46869A>C (FIRRM) | ||
| ENST00000609271.1:c.-201-2819T>G (SELE) | ENSP00000476784.1:n.-201-2819T>G |