Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94423059G>C , CM000669.2:g.94423059G>C | GRCh38 |
| NC_000007.13:g.94052371G>C , CM000669.1:g.94052371G>C | GRCh37 |
| NC_000007.12:g.93890307G>C | NCBI36 |
| NG_007405.1:g.33499G>C , LRG_2:g.33499G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.2506G>C MANE Select | ENSP00000297268.6:p.Ala836Pro | |
| ENST00000297268.10:c.2506G>C | ENSP00000297268.6:p.Ala836Pro | |
| ENST00000481570.5:n.589G>C | ||
| ENST00000497316.5:n.903G>C | ||
| ENST00000620463.1:c.2500G>C | ENSP00000477719.1:p.Ala834Pro | |
| NM_000089.3:c.2506G>C , LRG_2t1:c.2506G>C | NP_000080.2:p.Ala836Pro | |
| NM_000089.4:c.2506G>C MANE Select | NP_000080.2:p.Ala836Pro |