Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.41741181T= , CM000683.2:g.41741181T= | GRCh38 |
| NC_000021.8:g.43161341T= , CM000683.1:g.43161341T= | GRCh37 |
| NC_000021.7:g.42034410T= | NCBI36 |
| NG_032113.1:g.30909A= | |
| NG_032113.2:g.30909A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000332512.8:c.2012A= MANE Select | ENSP00000332454.3:p.Tyr671= | |
| ENST00000332512.7:c.2012A= | ENSP00000332454.3:p.Tyr671= | |
| ENST00000352483.3:c.2156A= | ENSP00000330161.2:p.Tyr719= | |
| NM_020639.2:c.2012A= | NP_065690.2:p.Tyr671= | |
| NM_020639.3:c.2012A= MANE Select | NP_065690.2:p.Tyr671= |