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