Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10648021C>A , CM000682.2:g.10648021C>A | GRCh38 |
| NC_000020.10:g.10628669C>A , CM000682.1:g.10628669C>A | GRCh37 |
| NC_000020.9:g.10576669C>A | NCBI36 |
| NG_007496.1:g.31026G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000214.3:c.1659G>T MANE Select | NP_000205.1:p.Glu553Asp |
| ENST00000254958.10:c.1659G>T MANE Select | ENSP00000254958.4:p.Glu553Asp |
| NM_000214.2:c.1659G>T | NP_000205.1:p.Glu553Asp |
| ENST00000254958.9:c.1659G>T | ENSP00000254958.4:p.Glu553Asp |
| ENST00000423891.6:n.1525G>T | |
| ENST00000613518.1:c.8G>T | |
| ENST00000617965.2:n.2248G>T | |
| ENST00000620743.1:n.716G>T | |
| ENST00000622545.1:c.390G>T |