Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4816597T>G , CM000681.2:g.4816597T>G | GRCh38 |
| NC_000019.9:g.4816609T>G , CM000681.1:g.4816609T>G | GRCh37 |
| NC_000019.8:g.4767609T>G | NCBI36 |
| NG_031998.1:g.20146A>C , LRG_358:g.20146A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248244.6:c.1781A>C MANE Select | ENSP00000248244.4:p.His594Pro | |
| ENST00000248244.5:c.1781A>C | ENSP00000248244.4:p.His594Pro | |
| ENST00000621756.1:c.1364A>C | ENSP00000479467.1:p.His455Pro | |
| NM_182919.3:c.1781A>C , LRG_358t1:c.1781A>C | NP_891549.1:p.His594Pro | |
| NM_001385678.1:c.1739A>C | NP_001372607.1:p.His580Pro | |
| NM_001385679.1:c.1646A>C | NP_001372608.1:p.His549Pro | |
| NM_001385680.1:c.1139A>C | NP_001372609.1:p.His380Pro | |
| NM_182919.4:c.1781A>C MANE Select | NP_891549.1:p.His594Pro |