Canonical Allele Identifier:
CA2467796141
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.634798G= , CM000686.2:g.634798G= | GRCh38 |
| NC_000024.9:g.545533G= , CM000686.1:g.545533G= | GRCh37 |
| NC_000024.8:g.515533G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000711141.1:c.458G= | ENSP00000518639.1:p.Arg153= | |
| ENST00000711142.1:c.458G= | ENSP00000518640.1:p.Arg153= | |
| ENST00000711143.1:c.458G= | ENSP00000518641.1:p.Arg153= | |
| ENST00000711145.1:c.458G= | ENSP00000518642.1:p.Arg153= |