Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.102503872T= , CM000672.2:g.102503872T= | GRCh38 |
| NC_000010.10:g.104263629T= , CM000672.1:g.104263629T= | GRCh37 |
| NC_000010.9:g.104253619T= | NCBI36 |
| NG_011901.1:g.3884A= | |
| NG_021338.1:g.4911T= , LRG_521:g.4911T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011539859.1:c.-29-252T= | XP_011538161.1:n.-29-252T= | |
| XM_011539863.1:c.8+886T= | XP_011538165.1:n.8+886T= | |
| XM_011539863.3:c.8+886T= | XP_011538165.1:n.8+886T= |