Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.70179265G= , CM000679.2:g.70179265G= | GRCh38 |
| NC_000017.10:g.68175406G= , CM000679.1:g.68175406G= | GRCh37 |
| NC_000017.9:g.65687001G= | NCBI36 |
| NG_008798.1:g.14731G= , LRG_328:g.14731G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000243457.4:c.*2942G= MANE Select | ENSP00000243457.2:n.*2942G= | |
| ENST00000243457.3:c.*2942G= | ENSP00000243457.2:n.*2942G= | |
| NM_000891.2:c.*2942G= , LRG_328t1:c.*2942G= | NP_000882.1:n.*2942G= | |
| NM_000891.3:c.*2942G= MANE Select | NP_000882.1:n.*2942G= |