Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.33124441G>A , CM000665.2:g.33124441G>A | GRCh38 |
| NC_000003.11:g.33165933G>A , CM000665.1:g.33165933G>A | GRCh37 |
| NC_000003.10:g.33140937G>A | NCBI36 |
| NG_008122.1:g.15484G>A , LRG_4:g.15484G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006371.5:c.655G>A MANE Select | NP_006362.1:p.Gly219Ser |
| ENST00000320954.11:c.655G>A MANE Select | ENSP00000323696.5:p.Gly219Ser |
| NM_001393363.1:c.655G>A | NP_001380292.1:p.Gly219Ser |
| NM_001393364.1:c.655G>A | NP_001380293.1:p.Gly219Ser |
| NM_001393365.1:c.505G>A | NP_001380294.1:p.Gly169Ser |
| NM_006371.4:c.655G>A , LRG_4t1:c.655G>A | NP_006362.1:p.Gly219Ser |
| ENST00000320954.10:c.655G>A | ENSP00000323696.5:p.Gly219Ser |
| ENST00000449224.1:c.655G>A | ENSP00000409997.1:p.Gly219Ser |
| ENST00000485310.1:n.249G>A |