Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.81357925T>C , CM000678.2:g.81357925T>C | GRCh38 |
| NC_000016.9:g.81391530T>C , CM000678.1:g.81391530T>C | GRCh37 |
| NC_000016.8:g.79949031T>C | NCBI36 |
| NG_009007.1:g.47960T>C , LRG_242:g.47960T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648349.2:c.*675T>C | ENSP00000498114.1:n.*675T>C | |
| ENST00000648994.2:c.967T>C MANE Select | ENSP00000497351.1:p.Ser323Pro | |
| ENST00000650388.1:c.501T>C | ENSP00000498081.1:n.501T>C | |
| ENST00000568107.2:c.967T>C | ENSP00000476795.1:p.Ser323Pro | |
| NM_022041.3:c.967T>C , LRG_242t1:c.967T>C | NP_071324.1:p.Ser323Pro | |
| XM_017023734.1:c.328T>C | XP_016879223.1:p.Ser110Pro | |
| NM_001377486.1:c.328T>C | NP_001364415.1:p.Ser110Pro | |
| NM_022041.4:c.967T>C MANE Select | NP_071324.1:p.Ser323Pro |