Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.21658298G= , CM000684.2:g.21658298G= | GRCh38 |
| NC_000022.10:g.22012587G= , CM000684.1:g.22012587G= | GRCh37 |
| NC_000022.9:g.20342587G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641967.1:n.195G= | ||
| ENST00000498589.1:n.375G= | ||
| XM_017029165.1:c.510G= | XP_016884654.1:p.Leu170= | |
| NR_169729.1:n.1110G= | ||
| NR_169730.1:n.1013G= | ||
| NR_169731.1:n.432-2539G= | ||
| NR_169732.1:n.164G= | ||
| NR_169733.1:n.222G= | ||
| NR_169734.1:n.246G= |