Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94941830T= , CM000672.2:g.94941830T= | GRCh38 |
| NC_000010.10:g.96701587T= , CM000672.1:g.96701587T= | GRCh37 |
| NC_000010.9:g.96691577T= | NCBI36 |
| NG_008385.1:g.8173T= | |
| NG_008385.2:g.8673T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.169-28T= MANE Select | ENSP00000260682.6:n.169-28T= | |
| ENST00000643112.1:c.169-28T= | ENSP00000496202.1:n.169-28T= | |
| ENST00000645207.1:n.294T= | ||
| ENST00000260682.6:c.169-28T= | ENSP00000260682.6:n.169-28T= | |
| ENST00000461906.1:n.194-28T= | ||
| NM_000771.3:c.169-28T= | NP_000762.2:n.169-28T= | |
| NM_000771.4:c.169-28T= MANE Select | NP_000762.2:n.169-28T= |