Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18786129T>G , CM000681.2:g.18786129T>G | GRCh38 |
| NC_000019.9:g.18896939T>G , CM000681.1:g.18896939T>G | GRCh37 |
| NC_000019.8:g.18757939T>G | NCBI36 |
| NG_007070.1:g.10176A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.1325A>C MANE Select | ENSP00000222271.2:p.Gln442Pro | |
| ENST00000222271.6:c.1325A>C | ENSP00000222271.2:p.Gln442Pro | |
| ENST00000425807.1:c.1166A>C | ENSP00000403792.1:p.Gln389Pro | |
| ENST00000542601.6:c.1226A>C | ENSP00000439156.2:p.Gln409Pro | |
| ENST00000612179.1:n.575A>C | ||
| NM_000095.2:c.1325A>C | NP_000086.2:p.Gln442Pro | |
| NM_000095.3:c.1325A>C MANE Select | NP_000086.2:p.Gln442Pro |