Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.111071652T= , CM000667.2:g.111071652T= | GRCh38 |
| NC_000005.9:g.110407350T= , CM000667.1:g.110407350T= | GRCh37 |
| NC_000005.8:g.110435249T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000420978.6:c.34+135T= | ENSP00000399099.2:n.34+135T= | |
| NR_045089.1:n.1438+135T= | ||
| NR_045089.2:n.1456+135T= |