Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.34255389G>C , CM000679.2:g.34255389G>C | GRCh38 |
| NC_000017.10:g.32582408G>C , CM000679.1:g.32582408G>C | GRCh37 |
| NC_000017.9:g.29606521G>C | NCBI36 |
| NG_012123.1:g.5113G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000580907.6:c.40G>C | ENSP00000462156.1:p.Ala14Pro | |
| ENST00000624362.2:n.105G>C | ||
| ENST00000225831.4:c.40G>C MANE Select | ENSP00000225831.4:p.Ala14Pro | |
| ENST00000580907.5:c.40G>C | ENSP00000462156.1:p.Ala14Pro | |
| ENST00000624362.1:n.172G>C | ||
| NM_002982.3:c.40G>C | NP_002973.1:p.Ala14Pro | |
| NM_002982.4:c.40G>C MANE Select | NP_002973.1:p.Ala14Pro |