Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169742185T= , CM000663.2:g.169742185T= | GRCh38 |
| NC_000001.10:g.169711326T= , CM000663.1:g.169711326T= | GRCh37 |
| NC_000001.9:g.167977950T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000498289.5:n.852-41626T= (FIRRM) | ||
| ENST00000609271.1:c.-201-8062A= (SELE) | ENSP00000476784.1:n.-201-8062A= |