Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160136665T= , CM000663.2:g.160136665T= | GRCh38 |
| NC_000001.10:g.160106455T= , CM000663.1:g.160106455T= | GRCh37 |
| NC_000001.9:g.158373079T= | NCBI36 |
| NG_008014.1:g.25908T= , LRG_6:g.25908T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000702.4:c.2659T= MANE Select | NP_000693.1:p.Trp887= |
| ENST00000361216.8:c.2659T= MANE Select | ENSP00000354490.3:p.Trp887= |
| NM_000702.3:c.2659T= | NP_000693.1:p.Trp887= |
| ENST00000361216.7:c.2659T= | ENSP00000354490.3:p.Trp887= |
| ENST00000392233.7:c.2659T= | ENSP00000376066.3:p.Trp887= |
| ENST00000447527.1:c.1740T= | |
| ENST00000472488.5:n.2762T= |