Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.1612721T= , CM000668.2:g.1612721T= | GRCh38 |
| NC_000006.11:g.1612956T= , CM000668.1:g.1612956T= | GRCh37 |
| NC_000006.10:g.1557955T= | NCBI36 |
| NG_009368.1:g.7276T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645831.2:c.*614T= MANE Select | ENSP00000493906.1:n.*614T= | |
| ENST00000380874.3:c.*614T= | ENSP00000370256.2:n.*614T= | |
| NM_001453.2:c.2276T= | NP_001444.2:n.2276T= | |
| NM_001453.3:c.*614T= MANE Select | NP_001444.2:n.*614T= |