Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.207454348T= , CM000663.2:g.207454348T= | GRCh38 |
| NC_000001.10:g.207627693T= , CM000663.1:g.207627693T= | GRCh37 |
| NC_000001.9:g.205694316T= | NCBI36 |
| NG_013006.1:g.5049T= , LRG_348:g.5049T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001006658.3:c.-71T= MANE Select | NP_001006659.1:n.-71T= |
| ENST00000367057.8:c.-71T= MANE Select | ENSP00000356024.3:n.-71T= |
| NM_001006658.2:c.-71T= , LRG_348t1:c.-71T= | NP_001006659.1:n.-71T= |
| NM_001877.4:c.-71T= | NP_001868.2:n.-71T= |
| NM_001877.5:c.-71T= | NP_001868.2:n.-71T= |
| ENST00000367057.7:c.-71T= | ENSP00000356024.3:n.-71T= |
| ENST00000367058.7:c.-71T= | ENSP00000356025.3:n.-71T= |
| ENST00000367059.3:c.-71T= | ENSP00000356026.3:n.-71T= |
| ENST00000699640.1:c.-385+1253T= | ENSP00000514493.1:n.-385+1253T= |