Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.6588403C>T , CM000671.2:g.6588403C>T | GRCh38 |
| NC_000009.11:g.6588403C>T , CM000671.1:g.6588403C>T | GRCh37 |
| NC_000009.10:g.6578403C>T | NCBI36 |
| NG_016397.1:g.62290G>A , LRG_643:g.62290G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000170.3:c.1705G>A MANE Select | NP_000161.2:p.Ala569Thr |
| ENST00000321612.8:c.1705G>A MANE Select | ENSP00000370737.4:p.Ala569Thr |
| NM_000170.2:c.1705G>A , LRG_643t1:c.1705G>A | NP_000161.2:p.Ala569Thr |
| ENST00000321612.6:c.1705G>A | ENSP00000370737.3:p.Ala569Thr |
| ENST00000639364.1:n.1405G>A | |
| ENST00000639443.1:n.1273G>A | |
| ENST00000639954.1:n.1413G>A | |
| ENST00000640592.1:n.1588G>A |