Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189035112T>G , CM000664.2:g.189035112T>G | GRCh38 |
| NC_000002.11:g.189899838T>G , CM000664.1:g.189899838T>G | GRCh37 |
| NC_000002.10:g.189608083T>G | NCBI36 |
| NG_011799.1:g.149768A>C | |
| NG_011799.2:g.149768A>C | |
| NG_011799.3:g.195190A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374866.9:c.4157A>C MANE Select | ENSP00000364000.3:p.Gln1386Pro | |
| ENST00000374866.7:c.4157A>C | ENSP00000364000.3:p.Gln1386Pro | |
| ENST00000618828.1:c.2996A>C | ENSP00000482184.1:p.Gln999Pro | |
| NM_000393.3:c.4157A>C | NP_000384.2:p.Gln1386Pro | |
| XM_011510573.1:c.4019A>C | XP_011508875.1:p.Gln1340Pro | |
| NM_000393.4:c.4157A>C | NP_000384.2:p.Gln1386Pro | |
| XM_011510573.3:c.4019A>C | XP_011508875.1:p.Gln1340Pro | |
| NM_000393.5:c.4157A>C MANE Select | NP_000384.2:p.Gln1386Pro |