Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48503838T= , CM000677.2:g.48503838T= | GRCh38 |
| NC_000015.9:g.48796035T= , CM000677.1:g.48796035T= | GRCh37 |
| NC_000015.8:g.46583327T= | NCBI36 |
| NG_008805.2:g.146951A= , LRG_778:g.146951A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.2062A= | ENSP00000453958.2:p.Thr688= | |
| ENST00000674301.2:c.2062A= | ENSP00000501333.2:p.Thr688= | |
| ENST00000684448.1:n.736A= | ||
| ENST00000316623.10:c.2062A= MANE Select | ENSP00000325527.5:p.Thr688= | |
| ENST00000316623.9:c.2062A= | ENSP00000325527.5:p.Thr688= | |
| ENST00000537463.6:c.637-29188A= | ENSP00000440294.2:n.637-29188A= | |
| NM_000138.4:c.2062A= , LRG_778t1:c.2062A= | NP_000129.3:p.Thr688= | |
| NM_000138.5:c.2062A= MANE Select | NP_000129.3:p.Thr688= |