Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.73442364G>C , CM000666.2:g.73442364G>C | GRCh38 |
| NC_000004.11:g.74308081G>C , CM000666.1:g.74308081G>C | GRCh37 |
| NC_000004.10:g.74526945G>C | NCBI36 |
| NG_023028.1:g.11149G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395792.7:c.551G>C MANE Select | ENSP00000379138.2:p.Arg184Pro | |
| ENST00000226359.2:c.551G>C | ENSP00000226359.2:p.Arg184Pro | |
| ENST00000395792.6:c.551G>C | ENSP00000379138.2:p.Arg184Pro | |
| NM_001134.2:c.551G>C | NP_001125.1:p.Arg184Pro | |
| XM_011531704.1:c.548G>C | XP_011530006.1:p.Arg183Pro | |
| NM_001354717.1:c.77G>C | NP_001341646.1:p.Arg26Pro | |
| NM_001134.3:c.551G>C MANE Select | NP_001125.1:p.Arg184Pro | |
| NM_001354717.2:c.77G>C | NP_001341646.2:p.Arg26Pro |