Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.1613156G>A , CM000668.2:g.1613156G>A | GRCh38 |
| NC_000006.11:g.1613391G>A , CM000668.1:g.1613391G>A | GRCh37 |
| NC_000006.10:g.1558390G>A | NCBI36 |
| NG_009368.1:g.7711G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645831.2:c.*1049G>A MANE Select | ENSP00000493906.1:n.*1049G>A | |
| ENST00000380874.3:c.*1049G>A | ENSP00000370256.2:n.*1049G>A | |
| NM_001453.2:c.2711G>A | NP_001444.2:n.2711G>A | |
| NM_001453.3:c.*1049G>A MANE Select | NP_001444.2:n.*1049G>A |