Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.43928842T>C , CM000684.2:g.43928842T>C | GRCh38 |
| NC_000022.10:g.44324722T>C , CM000684.1:g.44324722T>C | GRCh37 |
| NC_000022.9:g.42656055T>C | NCBI36 |
| NG_008631.1:g.10104T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216180.8:c.439T>C MANE Select | ENSP00000216180.3:p.Phe147Leu | |
| ENST00000216180.7:c.439T>C | ENSP00000216180.3:p.Phe147Leu | |
| ENST00000406117.6:c.*71T>C | ENSP00000384668.2:n.*71T>C | |
| ENST00000423180.2:c.427T>C | ENSP00000397987.2:p.Phe143Leu | |
| ENST00000478713.1:n.473T>C | ||
| NM_025225.2:c.439T>C | NP_079501.2:p.Phe147Leu | |
| NM_025225.3:c.439T>C MANE Select | NP_079501.2:p.Phe147Leu |