Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.21658297T= , CM000684.2:g.21658297T= | GRCh38 |
| NC_000022.10:g.22012586T= , CM000684.1:g.22012586T= | GRCh37 |
| NC_000022.9:g.20342586T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641967.1:n.194T= | ||
| ENST00000498589.1:n.374T= | ||
| XM_017029165.1:c.509T= | XP_016884654.1:p.Leu170= | |
| NR_169729.1:n.1109T= | ||
| NR_169730.1:n.1012T= | ||
| NR_169731.1:n.432-2540T= | ||
| NR_169732.1:n.163T= | ||
| NR_169733.1:n.221T= | ||
| NR_169734.1:n.245T= |