Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.11491693T= , CM000670.2:g.11491693T= | GRCh38 |
| NC_000008.10:g.11349202T= , CM000670.1:g.11349202T= | GRCh37 |
| NC_000008.9:g.11386611T= | NCBI36 |
| NG_023543.1:g.2682T= | |
| NG_023543.2:g.2682T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696154.2:n.274+4526T= | ||
| ENST00000696154.1:c.-91+4526T= | ENSP00000512445.1:n.-91+4526T= | |
| ENST00000645242.1:c.-91+4526T= | ENSP00000494690.1:n.-91+4526T= |