Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94418497T= , CM000663.2:g.94418497T= | GRCh38 |
| NC_000001.10:g.94884053T= , CM000663.1:g.94884053T= | GRCh37 |
| NC_000001.9:g.94656641T= | NCBI36 |
| NG_008865.1:g.5121T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370214.9:c.19T= MANE Select | ENSP00000359233.4:p.Tyr7= | |
| ENST00000647998.2:c.19T= | ENSP00000497921.2:p.Tyr7= | |
| ENST00000315713.5:c.19T= | ENSP00000326880.5:p.Tyr7= | |
| ENST00000370214.8:c.19T= | ENSP00000359233.4:p.Tyr7= | |
| NM_001122674.1:c.19T= | NP_001116146.1:p.Tyr7= | |
| NM_002858.3:c.19T= | NP_002849.1:p.Tyr7= | |
| XM_006710802.2:c.19T= | XP_006710865.2:p.Tyr7= | |
| NM_002858.4:c.19T= MANE Select | NP_002849.1:p.Tyr7= | |
| NM_001122674.2:c.19T= | NP_001116146.1:p.Tyr7= |