Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.43928858G>C , CM000684.2:g.43928858G>C | GRCh38 |
| NC_000022.10:g.44324738G>C , CM000684.1:g.44324738G>C | GRCh37 |
| NC_000022.9:g.42656071G>C | NCBI36 |
| NG_008631.1:g.10120G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216180.8:c.455G>C MANE Select | ENSP00000216180.3:p.Ser152Thr | |
| ENST00000216180.7:c.455G>C | ENSP00000216180.3:p.Ser152Thr | |
| ENST00000406117.6:c.*87G>C | ENSP00000384668.2:n.*87G>C | |
| ENST00000423180.2:c.443G>C | ENSP00000397987.2:p.Ser148Thr | |
| ENST00000478713.1:n.489G>C | ||
| NM_025225.2:c.455G>C | NP_079501.2:p.Ser152Thr | |
| NM_025225.3:c.455G>C MANE Select | NP_079501.2:p.Ser152Thr |