Linked Data
dbSNP Id:
rs2143256811
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.72124182A>C , CM000679.2:g.72124182A>C | GRCh38 |
| NC_000017.10:g.70120323A>C , CM000679.1:g.70120323A>C | GRCh37 |
| NC_000017.9:g.67631918A>C | NCBI36 |
| NG_012490.1:g.8163A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000245479.3:c.1325A>C MANE Select | ENSP00000245479.2:p.Tyr442Ser | |
| ENST00000245479.2:c.1325A>C | ENSP00000245479.2:p.Tyr442Ser | |
| NM_000346.3:c.1325A>C | NP_000337.1:p.Tyr442Ser | |
| NM_000346.4:c.1325A>C MANE Select | NP_000337.1:p.Tyr442Ser |