Linked Data
dbSNP Id:
rs2146776187
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.43928768C>G , CM000684.2:g.43928768C>G | GRCh38 |
| NC_000022.10:g.44324648C>G , CM000684.1:g.44324648C>G | GRCh37 |
| NC_000022.9:g.42655981C>G | NCBI36 |
| NG_008631.1:g.10030C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216180.8:c.421-56C>G MANE Select | ENSP00000216180.3:n.421-56C>G | |
| ENST00000216180.7:c.421-56C>G | ENSP00000216180.3:n.421-56C>G | |
| ENST00000406117.6:c.*53-56C>G | ENSP00000384668.2:n.*53-56C>G | |
| ENST00000423180.2:c.409-56C>G | ENSP00000397987.2:n.409-56C>G | |
| ENST00000478713.1:n.455-56C>G | ||
| NM_025225.2:c.421-56C>G | NP_079501.2:n.421-56C>G | |
| NM_025225.3:c.421-56C>G MANE Select | NP_079501.2:n.421-56C>G |