Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160127592G= , CM000663.2:g.160127592G= | GRCh38 |
| NC_000001.10:g.160097382G= , CM000663.1:g.160097382G= | GRCh37 |
| NC_000001.9:g.158364006G= | NCBI36 |
| NG_008014.1:g.16835G= , LRG_6:g.16835G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361216.8:c.789G= MANE Select | ENSP00000354490.3:p.Thr263= | |
| ENST00000361216.7:c.789G= | ENSP00000354490.3:p.Thr263= | |
| ENST00000392233.7:c.789G= | ENSP00000376066.3:p.Thr263= | |
| ENST00000472488.5:n.892G= | ||
| NM_000702.3:c.789G= | NP_000693.1:p.Thr263= | |
| NM_000702.4:c.789G= MANE Select | NP_000693.1:p.Thr263= |