Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160135510T= , CM000663.2:g.160135510T= | GRCh38 |
| NC_000001.10:g.160105300T= , CM000663.1:g.160105300T= | GRCh37 |
| NC_000001.9:g.158371924T= | NCBI36 |
| NG_008014.1:g.24753T= , LRG_6:g.24753T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000702.4:c.2192T= MANE Select | NP_000693.1:p.Met731= |
| ENST00000361216.8:c.2192T= MANE Select | ENSP00000354490.3:p.Met731= |
| NM_000702.3:c.2192T= | NP_000693.1:p.Met731= |
| ENST00000361216.7:c.2192T= | ENSP00000354490.3:p.Met731= |
| ENST00000392233.7:c.2192T= | ENSP00000376066.3:p.Met731= |
| ENST00000447527.1:c.1324T= | |
| ENST00000472488.5:n.2295T= |