Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32276850T= , CM000668.2:g.32276850T= | GRCh38 |
| NC_000006.11:g.32244627T= , CM000668.1:g.32244627T= | GRCh37 |
| NC_000006.10:g.32352605T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NR_136244.1:n.440+14041T= | |
| NR_136245.1:n.242+21436T= | |
| NR_136246.1:n.242+21436T= | |
| XM_011515039.1:c.421+14041T= | XP_011513341.1:n.421+14041T= |
| XM_011515040.1:c.421+14041T= | XP_011513342.1:n.421+14041T= |