Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.59030427T= , CM000682.2:g.59030427T= | GRCh38 |
| NC_000020.10:g.57605482T= , CM000682.1:g.57605482T= | GRCh37 |
| NC_000020.9:g.57038877T= | NCBI36 |
| NG_031871.1:g.6941A= | |
| NG_031871.2:g.6941A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006886.4:c.35A= MANE Select | NP_008817.1:p.Tyr12= |
| ENST00000243997.8:c.35A= MANE Select | ENSP00000243997.3:p.Tyr12= |
| NM_006886.3:c.35A= | NP_008817.1:p.Tyr12= |
| NR_037929.1:n.739A= | |
| NR_037930.1:n.480A= | |
| ENST00000243997.7:c.35A= | ENSP00000243997.3:p.Tyr12= |
| ENST00000395659.1:c.35A= | ENSP00000379019.1:p.Tyr12= |
| ENST00000395663.1:c.35A= | ENSP00000379023.1:p.Tyr12= |