Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.1611771G>A , CM000668.2:g.1611771G>A | GRCh38 |
| NC_000006.11:g.1612006G>A , CM000668.1:g.1612006G>A | GRCh37 |
| NC_000006.10:g.1557005G>A | NCBI36 |
| NG_009368.1:g.6326G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001453.3:c.1326G>A MANE Select | NP_001444.2:p.Ser442= |
| ENST00000645831.2:c.1326G>A MANE Select | ENSP00000493906.1:p.Ser442= |
| NM_001453.2:c.1326G>A | NP_001444.2:p.Ser442= |
| ENST00000380874.3:c.1326G>A | ENSP00000370256.2:p.Ser442= |