Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48485397A>G , CM000677.2:g.48485397A>G | GRCh38 |
| NC_000015.9:g.48777594A>G , CM000677.1:g.48777594A>G | GRCh37 |
| NC_000015.8:g.46564886A>G | NCBI36 |
| NG_008805.2:g.165392T>C , LRG_778:g.165392T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000138.5:c.3689T>C MANE Select | NP_000129.3:p.Met1230Thr |
| ENST00000316623.10:c.3689T>C MANE Select | ENSP00000325527.5:p.Met1230Thr |
| NM_000138.4:c.3689T>C , LRG_778t1:c.3689T>C | NP_000129.3:p.Met1230Thr |
| ENST00000316623.9:c.3689T>C | ENSP00000325527.5:p.Met1230Thr |
| ENST00000537463.6:c.637-10747T>C | ENSP00000440294.2:n.637-10747T>C |
| ENST00000559133.6:c.3689T>C | ENSP00000453958.2:p.Met1230Thr |
| ENST00000674301.2:c.3689T>C | ENSP00000501333.2:p.Met1230Thr |
| ENST00000684448.1:n.2363T>C |