Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.11309964A>G , CM000678.2:g.11309964A>G | GRCh38 |
| NC_000016.9:g.11403821A>G , CM000678.1:g.11403821A>G | GRCh37 |
| NC_000016.8:g.11311322A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000649869.1:n.152+60186A>G | ||
| ENST00000572173.1:c.-436-2865A>G | ENSP00000461206.1:n.-436-2865A>G | |
| ENST00000573910.1:n.161-6488A>G | ||
| XR_933070.1:n.733+60186A>G | ||
| XR_933070.3:n.876+60186A>G |