Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31268985T>C , CM000668.2:g.31268985T>C | GRCh38 |
| NC_000006.11:g.31236762T>C , CM000668.1:g.31236762T>C | GRCh37 |
| NC_000006.10:g.31344741T>C | NCBI36 |
| NG_029422.2:g.8147A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000376228.10:c.*184A>G MANE Select | ENSP00000365402.5:n.*184A>G | |
| ENST00000376228.9:c.*184A>G | ENSP00000365402.5:n.*184A>G | |
| ENST00000376237.8:c.*872A>G | ENSP00000365412.4:n.*872A>G | |
| ENST00000383329.7:c.*184A>G | ENSP00000372819.3:n.*184A>G | |
| ENST00000466892.5:n.518A>G | ||
| ENST00000470363.5:n.1043A>G | ||
| ENST00000487245.5:n.1644A>G | ||
| NM_002117.5:c.*184A>G | NP_002108.4:n.*184A>G | |
| NM_002117.6:c.*184A>G MANE Select | NP_002108.4:n.*184A>G |