Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50578924T= , CM000684.2:g.50578924T= | GRCh38 |
| NC_000022.10:g.51017353T= , CM000684.1:g.51017353T= | GRCh37 |
| NC_000022.9:g.49364219T= | NCBI36 |
| NG_012643.1:g.4744A= | |
| NG_029213.1:g.9076A= , LRG_855:g.9076A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452668.1:n.319+112A= | ||
| ENST00000453634.5:c.328+112A= | ENSP00000457031.1:n.328+112A= | |
| ENST00000492556.5:n.2189+112A= | ||
| NR_027928.2:n.1551+112A= |