Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.33979179C>A , CM000679.2:g.33979179C>A | GRCh38 |
| NC_000017.10:g.32306198C>A , CM000679.1:g.32306198C>A | GRCh37 |
| NC_000017.9:g.29330311C>A | NCBI36 |
| NG_029763.1:g.182628G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000359872.6:c.555+176799G>T | ENSP00000352934.6:n.555+176799G>T | |
| NM_001094.4:c.555+176799G>T | NP_001085.2:n.555+176799G>T | |
| XR_001752840.1:n.404+7966G>T | ||
| NM_001094.5:c.555+176799G>T | NP_001085.2:n.555+176799G>T |