Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48425401T= , CM000677.2:g.48425401T= | GRCh38 |
| NC_000015.9:g.48717598T= , CM000677.1:g.48717598T= | GRCh37 |
| NC_000015.8:g.46504890T= | NCBI36 |
| NG_008805.2:g.225388A= , LRG_778:g.225388A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.*229A= | ENSP00000453958.2:n.*229A= | |
| ENST00000674301.2:c.*934A= | ENSP00000501333.2:n.*934A= | |
| ENST00000682170.1:n.1602A= | ||
| ENST00000682767.1:n.718A= | ||
| ENST00000316623.10:c.7421A= MANE Select | ENSP00000325527.5:p.Tyr2474= | |
| ENST00000674301.1:c.2587A= | ENSP00000501333.1:n.2587A= | |
| ENST00000316623.9:c.7421A= | ENSP00000325527.5:p.Tyr2474= | |
| ENST00000559133.5:c.2790A= | ||
| NM_000138.4:c.7421A= , LRG_778t1:c.7421A= | NP_000129.3:p.Tyr2474= | |
| NM_000138.5:c.7421A= MANE Select | NP_000129.3:p.Tyr2474= |