Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48463977A>G , CM000677.2:g.48463977A>G | GRCh38 |
| NC_000015.9:g.48756174A>G , CM000677.1:g.48756174A>G | GRCh37 |
| NC_000015.8:g.46543466A>G | NCBI36 |
| NG_008805.2:g.186812T>C , LRG_778:g.186812T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000559133.6:c.4987T>C | ENSP00000453958.2:p.Cys1663Arg | |
| ENST00000674301.2:c.4987T>C | ENSP00000501333.2:p.Cys1663Arg | |
| ENST00000684448.1:n.3661T>C | ||
| ENST00000316623.10:c.4987T>C MANE Select | ENSP00000325527.5:p.Cys1663Arg | |
| ENST00000316623.9:c.4987T>C | ENSP00000325527.5:p.Cys1663Arg | |
| ENST00000537463.6:c.*750T>C | ENSP00000440294.2:n.*750T>C | |
| ENST00000559133.5:c.294T>C | ||
| NM_000138.4:c.4987T>C , LRG_778t1:c.4987T>C | NP_000129.3:p.Cys1663Arg | |
| NM_000138.5:c.4987T>C MANE Select | NP_000129.3:p.Cys1663Arg |