Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.6604709C>A , CM000671.2:g.6604709C>A | GRCh38 |
| NC_000009.11:g.6604709C>A , CM000671.1:g.6604709C>A | GRCh37 |
| NC_000009.10:g.6594709C>A | NCBI36 |
| NG_016397.1:g.45984G>T , LRG_643:g.45984G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000321612.8:c.937G>T MANE Select | ENSP00000370737.4:p.Ala313Ser | |
| ENST00000638654.1:c.184G>T | ENSP00000491101.1:p.Ala62Ser | |
| ENST00000639364.1:n.637G>T | ||
| ENST00000639443.1:n.505G>T | ||
| ENST00000639493.1:n.89G>T | ||
| ENST00000639954.1:n.645G>T | ||
| ENST00000640592.1:n.820G>T | ||
| ENST00000321612.6:c.937G>T | ENSP00000370737.3:p.Ala313Ser | |
| ENST00000463305.1:n.142+422G>T | ||
| NM_000170.2:c.937G>T , LRG_643t1:c.937G>T | NP_000161.2:p.Ala313Ser | |
| NM_000170.3:c.937G>T MANE Select | NP_000161.2:p.Ala313Ser |