Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57766157C>G , CM000674.2:g.57766157C>G | GRCh38 |
| NC_000012.11:g.58159940C>G , CM000674.1:g.58159940C>G | GRCh37 |
| NC_000012.10:g.56446207C>G | NCBI36 |
| NG_007076.1:g.6037G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000546609.2:n.148G>C | ||
| ENST00000713544.1:c.236G>C | ENSP00000518840.1:p.Ser79Thr | |
| ENST00000713545.1:c.236G>C | ENSP00000518841.1:p.Ser79Thr | |
| ENST00000228606.9:c.236G>C MANE Select | ENSP00000228606.4:p.Ser79Thr | |
| ENST00000228606.8:c.236G>C | ENSP00000228606.4:p.Ser79Thr | |
| ENST00000546496.1:n.64G>C | ||
| ENST00000546609.1:c.148G>C | ||
| ENST00000547344.5:n.290G>C | ||
| ENST00000552186.1:n.355G>C | ||
| NM_000785.3:c.236G>C | NP_000776.1:p.Ser79Thr | |
| NM_000785.4:c.236G>C MANE Select | NP_000776.1:p.Ser79Thr |