Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.35564779C= , CM000682.2:g.35564779C= | GRCh38 |
| NC_000020.10:g.34152695C= , CM000682.1:g.34152695C= | GRCh37 |
| NC_000020.9:g.33616109C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000674340.1:n.2113G= | ||
| ENST00000674470.1:n.1440G= | ||
| ENST00000611673.4:n.1134G= | ||
| ENST00000613061.4:n.1484G= | ||
| ENST00000615531.4:n.4649G= | ||
| ENST00000616711.4:n.1798G= | ||
| ENST00000621044.4:n.762G= | ||
| NR_119376.1:n.4661G= |