Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94423115T>C , CM000669.2:g.94423115T>C | GRCh38 |
| NC_000007.13:g.94052427T>C , CM000669.1:g.94052427T>C | GRCh37 |
| NC_000007.12:g.93890363T>C | NCBI36 |
| NG_007405.1:g.33555T>C , LRG_2:g.33555T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.2562T>C MANE Select | ENSP00000297268.6:p.Thr854= | |
| ENST00000297268.10:c.2562T>C | ENSP00000297268.6:p.Thr854= | |
| ENST00000481570.5:n.645T>C | ||
| ENST00000497316.5:n.959T>C | ||
| ENST00000620463.1:c.2556T>C | ENSP00000477719.1:p.Thr852= | |
| NM_000089.3:c.2562T>C , LRG_2t1:c.2562T>C | NP_000080.2:p.Thr854= | |
| NM_000089.4:c.2562T>C MANE Select | NP_000080.2:p.Thr854= |